| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:48088491-48088752 | Common:2; Rare:60 | ||||
| chr7:48088866-48089418 | Common:7; Rare:135 | ||||
| chr7:50450300-50450466 | Common:1; Rare:72 | ||||
| chr7:55365930-55366069 | Rare:61 | ||||
| chr7:55366251-55366388 | Common:1; Rare:58 | ||||
| chr7:55572320-55572587 | Common:1; Rare:103 | ||||
| chr7:55951737-55951942 | Rare:59 | ||||
| chr7:56034001-56034272 | Rare:79; Clinvar:1 | ||||
| chr7:56051136-56051242 | Rare:23; Clinvar:2 | ||||
| chr7:56051355-56051983 | Common:1; Rare:217; Clinvar:6; Clinvar (benign):1 | ||||
| chr7:56064176-56064378 | Common:2; Rare:122 | ||||
| chr7:56106362-56106691 | Common:8; Rare:121 | ||||
| chr7:64563038-64563191 | Common:1; Rare:42 | ||||
| chr7:64665985-64666176 | Common:4; Rare:43 | ||||
| chr7:65006669-65006856 | Common:2; Rare:51 |