| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:73069703-73069922 | Common:1; Rare:96 | ||||
| chr4:74157842-74158179 | Common:2; Rare:143 | ||||
| chr4:75514279-75514502 | Rare:76 | ||||
| chr4:75673291-75673566 | Common:1; Rare:106 | ||||
| chr4:75724367-75724813 | Common:2; Rare:132 | ||||
| chr4:76148370-76148556 | Common:3; Rare:59 | ||||
| chr4:76251606-76251739 | Rare:33 | ||||
| chr4:76949569-76949889 | Common:2; Rare:107 | ||||
| chr4:77075967-77076139 | Common:4; Rare:82 | ||||
| chr4:77862641-77862872 | Common:3; Rare:84 | ||||
| chr4:78057445-78057604 | Common:2; Rare:38 | ||||
| chr4:81471809-81472075 | Common:1; Rare:86 | ||||
| chr4:82373936-82374199 | Common:2; Rare:80 | ||||
| chr4:82429367-82429634 | Common:1; Rare:164; Clinvar:13; Clinvar (benign):5 | ||||
| chr4:82890980-82891316 | Common:1; Rare:123 |