| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:143513430-143513753 | Common:1; Rare:98 | ||||
| chr4:144140656-144140814 | Common:1; Rare:32 | ||||
| chr4:144645814-144646202 | Common:1; Rare:113 | ||||
| chr4:144646367-144646690 | Common:1; Rare:78 | ||||
| chr4:145098124-145098363 | Rare:78 | ||||
| chr4:145180441-145180855 | Common:1; Rare:118 | ||||
| chr4:145481563-145481767 | Rare:60 | ||||
| chr4:145482869-145483001 | Rare:21 | ||||
| chr4:145619346-145619402 | Rare:19 | ||||
| chr4:145938408-145938558 | Common:1; Rare:33 | ||||
| chr4:147480775-147481121 | Common:1; Rare:67 | ||||
| chr4:147617225-147617479 | Common:1; Rare:58 | ||||
| chr4:147684054-147684289 | Common:1; Rare:83 | ||||
| chr4:147732001-147732357 | Rare:132 | ||||
| chr4:148442323-148442732 | Rare:118; Clinvar:4; Clinvar (benign):3 |