| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139341197-139341369 | Rare:39 | ||||
| chr7:139359692-139359982 | Common:3; Rare:115 | ||||
| chr7:140696602-140696735 | Common:1; Rare:42 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738228-141738464 | Rare:93 | ||||
| chr7:142854989-142855138 | Common:2; Rare:44 | ||||
| chr7:148339137-148339562 | Common:9; Rare:101 | ||||
| chr7:149028586-149028894 | Common:5; Rare:110 | ||||
| chr7:149090682-149090870 | Rare:50 | ||||
| chr7:149126278-149126438 | Common:5; Rare:51 | ||||
| chr7:149195423-149195601 | Rare:45 | ||||
| chr7:150368535-150368854 | Common:1; Rare:92 | ||||
| chr7:150379061-150379327 | Common:2; Rare:93 | ||||
| chr7:151057856-151058229 | Common:4; Rare:102 | ||||
| chr7:151227162-151227378 | Common:1; Rare:59 |