First described in Toyota 1999
Table 1 from the publication
I re-mapped each marker to hg19(GRCh37) and hg18(NCBI36) builts based on GeneBank sequence ID provided in the publication. Coordinates were obtained from UCSC Genome Browser
| MINT | hg18 | hg19 | nearby gene |
|---|---|---|---|
| MINT1 | chr5:75,415,502-75,416,033 | chr5:75,379,746-75,380,277 | SV2C |
| MINT2 | chr2:58,508,470-58,509,030 | chr2:58,654,966-58,655,526 | none |
| MINT3 | chr1:32,992,445-32,993,007 | chr1:33,219,858-33,220,420 | KIAA1522 |
| MINT4 | chr15:94,703,691-94,704,172 | chr15:96,902,687-96,903,168 | none |
| MINT5 | chr14:56,340,986-56,341,835 | chr14:57,271,233-57,272,082 | OTX2 |
| MINT6 | chr12:63,505,392-63,505,734 | chr12:65,219,125-65,219,467 | KIAA0984/TBC1D30 |
| MINT7 | chr6:28,565,802-28,566,282 | chr6:28,457,823-28,458,303 | none/tRNA_Thr |
| MINT8 | chr11:31,804,495-31,805,098 | chr11:31,847,919-31,848,522 | PAX6/RCN1 |
| MINT9 | chr1:26,608,598-26,609,191 | chr1:26,736,011-26,736,604 | LIN28 |
| MINT10 | chr9:138,223,414-138,224,019 | chr9:139,083,593-139,084,198 | none/RBSG2 |
| MINT11 | chr5:82,803,493-82,804,128 | chr5:82,767,737-82,768,372 | VCAN |
| MINT12 | chr7:129,212,186-129,212,737 | chr7:129,424,950-129,425,501 | none |
| MINT13 | chr5:180,743,717-180,744,030 | chr5:180,811,111-180,811,424 | LINE1 |
| MINT14 | chr10:11,766,789-11,767,408 | chr10:11,726,783-11,727,402 | none |
| MINT15 | chr11:69,226,516-69,227,158 | chr11:69,517,335-69,517,977 | FGF19 |
| MINT16 | chr2:219,825,355-219,826,018 | chr2:220,117,111-220,117,774 | TUBA4A |
| MINT17 | chr12:115,801,316-115,801,794 | chr12:117,316,933-117,317,411 | HRK |
| MINT18 | chr17:23,834,101-23,834,312 | chr17:26,809,974-26,810,185 | SLC13A2 |
| MINT19 | chr20:36,662,950-36,663,391 | chr20:37,229,536-37,229,977 | ARHGAP40 |