| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:151232414-151232537 | Rare:41 | ||||
| chr7:151736450-151736622 | Rare:26 | ||||
| chr7:151877153-151877518 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:152435655-152435731 | Common:1; Rare:17 | ||||
| chr7:155002918-155002998 | Rare:27 | ||||
| chr7:155644377-155644804 | Common:4; Rare:139 | ||||
| chr7:156640541-156640685 | Common:3; Rare:76 | ||||
| chr7:157336697-157337128 | Common:5; Rare:197; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:158856423-158856716 | Common:7; Rare:104 | ||||
| chr8:232076-232468 | Common:3; Rare:156 | ||||
| chr8:2127530-2127804 | Common:13; Rare:64 | ||||
| chr8:6406527-6406670 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6563225-6563523 | Common:1; Rare:71 | ||||
| chr8:6708194-6708339 | Common:2; Rare:53 | ||||
| chr8:9150584-9150848 | Common:1; Rare:85 |