| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75673291-75673534 | Common:1; Rare:94 | ||||
| chr4:75724370-75724724 | Common:1; Rare:98 | ||||
| chr4:75990912-75991046 | Common:1; Rare:48 | ||||
| chr4:76148364-76148556 | Common:3; Rare:63 | ||||
| chr4:76251665-76251739 | Rare:20 | ||||
| chr4:76586145-76586292 | Common:2; Rare:21 | ||||
| chr4:76949622-76949897 | Common:1; Rare:83 | ||||
| chr4:77075943-77076105 | Common:3; Rare:90 | ||||
| chr4:77157966-77158175 | Common:1; Rare:75 | ||||
| chr4:77862650-77862889 | Common:3; Rare:96 | ||||
| chr4:78551651-78551820 | Rare:46 | ||||
| chr4:80183821-80183996 | Common:2; Rare:41 | ||||
| chr4:80197249-80197630 | Common:3; Rare:83 | ||||
| chr4:82373887-82374317 | Common:3; Rare:129 | ||||
| chr4:82429314-82429634 | Common:2; Rare:193; Clinvar:13; Clinvar (benign):7 |