| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:144284880-144285076 | Common:1; Rare:48 | ||||
| chr6:150683360-150683625 | Common:1; Rare:49 | ||||
| chr6:158043784-158043984 | Common:1; Rare:41 | ||||
| chr6:159693921-159694192 | Rare:42 | ||||
| chr6:160100802-160100849 | Common:1; Rare:3 | ||||
| chr6:166633784-166633935 | Common:1; Rare:32 | ||||
| chr6:166692900-166693178 | Common:2; Rare:41 | ||||
| chr6:167934535-167934810 | Common:2; Rare:51 | ||||
| chr7:149434-149840 | Common:9; Rare:144 | ||||
| chr7:604505-604647 | Common:4; Rare:41 | ||||
| chr7:2009072-2009239 | Common:1; Rare:52 | ||||
| chr7:5427821-5427891 | Rare:28 | ||||
| chr7:7689059-7689434 | Common:1; Rare:69 | ||||
| chr7:15688232-15688420 | Common:2; Rare:48 | ||||
| chr7:26193252-26193696 | Rare:156; Clinvar (benign):2 |