| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143386802-143386901 | Common:1; Rare:19 | ||||
| chr7:143388568-143388839 | Common:3; Rare:85 | ||||
| chr7:143429939-143430048 | Common:3; Rare:13 | ||||
| chr7:144256129-144256275 | Common:1; Rare:10 | ||||
| chr7:144647652-144647838 | Common:1; Rare:31 | ||||
| chr7:148807695-148807804 | Common:2; Rare:27; Clinvar (benign):1 | ||||
| chr7:149084084-149084343 | Common:1; Rare:47 | ||||
| chr7:149233149-149233294 | Common:1; Rare:20 | ||||
| chr7:149334622-149334844 | Rare:38 | ||||
| chr7:149486441-149486591 | Rare:27 | ||||
| chr7:149558648-149558695 | Rare:7 | ||||
| chr7:149571514-149571768 | Common:4; Rare:47 | ||||
| chr7:149839640-149840089 | Common:3; Rare:80 | ||||
| chr7:151029348-151029468 | Common:2; Rare:21 | ||||
| chr7:151218757-151219132 | Common:3; Rare:103 |