| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75673284-75673718 | Common:1; Rare:166 | ||||
| chr4:75724363-75724852 | Common:2; Rare:153 | ||||
| chr4:76147785-76147960 | Common:4; Rare:43 | ||||
| chr4:76148346-76148588 | Common:4; Rare:77 | ||||
| chr4:76213534-76214005 | Common:4; Rare:163; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:76251582-76251739 | Rare:36 | ||||
| chr4:76434986-76435255 | Common:4; Rare:52 | ||||
| chr4:76949618-76949873 | Common:1; Rare:73 | ||||
| chr4:77075965-77076105 | Common:3; Rare:72 | ||||
| chr4:77076258-77076340 | Common:2; Rare:38 | ||||
| chr4:77862635-77862902 | Common:3; Rare:106 | ||||
| chr4:78939263-78939515 | Common:2; Rare:105 | ||||
| chr4:80072714-80072851 | Common:1; Rare:35; Clinvar (benign):1 | ||||
| chr4:82373131-82373189 | Rare:25 | ||||
| chr4:82373881-82374338 | Common:3; Rare:144 |