| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:77199287-77199322 | Rare:9 | ||||
| chr7:77312161-77312422 | Common:2; Rare:60 | ||||
| chr7:77353003-77353197 | Common:2; Rare:60 | ||||
| chr7:77662860-77662993 | Common:4; Rare:40 | ||||
| chr7:87179328-87179663 | Common:1; Rare:59 | ||||
| chr7:87197975-87198115 | Rare:42 | ||||
| chr7:88218862-88219109 | Rare:66 | ||||
| chr7:91266914-91267225 | Common:1; Rare:68 | ||||
| chr7:92085348-92085522 | Rare:40 | ||||
| chr7:92113779-92114100 | Common:2; Rare:82 | ||||
| chr7:94392139-94392313 | Common:2; Rare:24 | ||||
| chr7:94396175-94396424 | Common:5; Rare:40 | ||||
| chr7:94398356-94398405 | Common:2; Rare:7; Clinvar (benign):2 | ||||
| chr7:94408180-94408380 | Common:1; Rare:55; Clinvar:3 | ||||
| chr7:94409318-94409822 | Common:4; Rare:136; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):2 |