| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:129611592-129611797 | Common:2; Rare:72 | ||||
| chr7:129952882-129953115 | Rare:68 | ||||
| chr7:130051329-130051505 | Common:1; Rare:62 | ||||
| chr7:130070232-130070572 | Common:3; Rare:92 | ||||
| chr7:130204830-130204940 | Rare:22 | ||||
| chr7:130205074-130205609 | Common:2; Rare:191 | ||||
| chr7:130345110-130345650 | Common:6; Rare:81 | ||||
| chr7:130417317-130417480 | Common:1; Rare:26 | ||||
| chr7:130439851-130440640 | Common:8; Rare:267 | ||||
| chr7:130440987-130441341 | Common:3; Rare:147; Clinvar:2; Clinvar (benign):2 | ||||
| chr7:130441527-130441938 | Rare:108 | ||||
| chr7:130490970-130491097 | Common:1; Rare:27 | ||||
| chr7:130491965-130492156 | Common:1; Rare:44 | ||||
| chr7:130492308-130493155 | Common:7; Rare:205 | ||||
| chr7:130668639-130668995 | Common:3; Rare:127 |