| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82561935-82562055 | Rare:33 | ||||
| chr4:82890936-82891280 | Common:1; Rare:118 | ||||
| chr4:82900397-82900821 | Common:1; Rare:130 | ||||
| chr4:82900909-82901023 | Rare:43 | ||||
| chr4:83012842-83013115 | Common:1; Rare:80 | ||||
| chr4:83034928-83035251 | Common:1; Rare:84 | ||||
| chr4:83455772-83456093 | Common:3; Rare:125 | ||||
| chr4:83485068-83485287 | Common:3; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:83535989-83536327 | Common:1; Rare:91 | ||||
| chr4:84966640-84967036 | Rare:101 | ||||
| chr4:85827497-85827645 | Common:1; Rare:23 | ||||
| chr4:85827693-85827963 | Common:1; Rare:40 | ||||
| chr4:85930051-85930273 | Common:2; Rare:47 | ||||
| chr4:86101900-86102196 | Rare:53; Clinvar (benign):1 | ||||
| chr4:86593991-86594401 | Rare:118 |