| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:47979469-47979719 | Rare:101 | ||||
| chr7:48088842-48089245 | Common:4; Rare:98 | ||||
| chr7:49773467-49773678 | Rare:61 | ||||
| chr7:50450306-50450453 | Common:1; Rare:59 | ||||
| chr7:55365919-55366090 | Rare:74 | ||||
| chr7:55572341-55572553 | Common:1; Rare:88 | ||||
| chr7:55887387-55887671 | Common:5; Rare:98 | ||||
| chr7:55951739-55951940 | Rare:58 | ||||
| chr7:56051429-56051845 | Common:1; Rare:159; Clinvar:5; Clinvar (benign):1 | ||||
| chr7:56064176-56064324 | Common:2; Rare:90 | ||||
| chr7:56092924-56093209 | Common:2; Rare:53 | ||||
| chr7:56106367-56106565 | Common:6; Rare:85 | ||||
| chr7:64307223-64307464 | Common:3; Rare:64 | ||||
| chr7:64562984-64563252 | Common:4; Rare:80 | ||||
| chr7:64794267-64794456 | Common:3; Rare:54 |