| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:139359690-139359968 | Common:2; Rare:114 | ||||
| chr7:140177021-140177332 | Common:3; Rare:113 | ||||
| chr7:141551284-141551428 | Common:1; Rare:44; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738027-141738464 | Common:4; Rare:133 | ||||
| chr7:142854827-142855190 | Common:5; Rare:106 | ||||
| chr7:143288165-143288457 | Common:1; Rare:109 | ||||
| chr7:143380954-143381131 | Rare:50 | ||||
| chr7:143902121-143902292 | Common:5; Rare:55 | ||||
| chr7:149090676-149090897 | Rare:60 | ||||
| chr7:149126234-149126438 | Common:6; Rare:68 | ||||
| chr7:150379084-150379317 | Common:1; Rare:76 | ||||
| chr7:150800315-150800487 | Common:4; Rare:50 | ||||
| chr7:150800499-150800811 | Common:3; Rare:70 | ||||
| chr7:151028195-151028490 | Rare:112 | ||||
| chr7:151062867-151063135 | Common:2; Rare:56 |