| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:159727333-159727666 | Common:5; Rare:136 | ||||
| chr6:159789517-159790014 | Common:5; Rare:168 | ||||
| chr6:159790259-159790559 | Common:8; Rare:106 | ||||
| chr6:166342519-166342657 | Common:3; Rare:52 | ||||
| chr6:166999061-166999415 | Common:1; Rare:120 | ||||
| chr6:169702009-169702138 | Common:1; Rare:52 | ||||
| chr6:169751521-169751645 | Rare:45; Clinvar (benign):1 | ||||
| chr6:170554219-170554417 | Common:1; Rare:64 | ||||
| chr7:727252-727293 | Rare:12; Clinvar:1 | ||||
| chr7:1570018-1570102 | Common:1; Rare:26 | ||||
| chr7:2242171-2242261 | Common:2; Rare:53 | ||||
| chr7:4775478-4775652 | Common:6; Rare:74; Clinvar:1 | ||||
| chr7:6009029-6009355 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):15 | ||||
| chr7:6104675-6105002 | Common:5; Rare:109 | ||||
| chr7:17940449-17940584 | Common:1; Rare:60 |