| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:30504570-30504647 | Rare:27 | ||||
| chr7:30504720-30505090 | Common:4; Rare:123 | ||||
| chr7:30594706-30595157 | Common:8; Rare:193; Clinvar:11; Clinvar (benign):16 | ||||
| chr7:30752010-30752142 | Common:1; Rare:31 | ||||
| chr7:32071008-32071285 | Common:2; Rare:56 | ||||
| chr7:32071399-32071476 | Rare:11 | ||||
| chr7:32495238-32495587 | Rare:90 | ||||
| chr7:32495904-32496011 | Rare:19 | ||||
| chr7:32892129-32892237 | Rare:24 | ||||
| chr7:32957221-32957502 | Common:2; Rare:78 | ||||
| chr7:32957540-32957781 | Rare:67 | ||||
| chr7:32957815-32958044 | Common:3; Rare:55 | ||||
| chr7:33063116-33063236 | Common:1; Rare:42 | ||||
| chr7:33109230-33109513 | Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:33129526-33129665 | Common:1; Rare:39; Clinvar:4; Clinvar (benign):1 |