| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:51316716-51316962 | Common:7; Rare:155 | ||||
| chr7:54759070-54759440 | Common:9; Rare:299 | ||||
| chr7:55018709-55019290 | Common:5; Rare:242; Clinvar:3; Clinvar (benign):3 | ||||
| chr7:55365370-55365740 | Common:7; Rare:189 | ||||
| chr7:55365844-55366093 | Rare:172 | ||||
| chr7:55366130-55366470 | Common:5; Rare:221 | ||||
| chr7:55571570-55572060 | Common:3; Rare:205 | ||||
| chr7:55572442-55572765 | Common:4; Rare:154 | ||||
| chr7:55887500-55887808 | Common:23; Rare:194 | ||||
| chr7:55951721-55951951 | Rare:123 | ||||
| chr7:55964748-55965019 | Common:2; Rare:110 | ||||
| chr7:56034018-56034490 | Common:1; Rare:184; Clinvar:1 | ||||
| chr7:56051364-56051858 | Common:2; Rare:364; Clinvar:10; Clinvar (benign):2 | ||||
| chr7:56064185-56064369 | Common:3; Rare:216 | ||||
| chr7:56106367-56106715 | Common:14; Rare:192 |