| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82429320-82429631 | Common:2; Rare:191; Clinvar:12; Clinvar (benign):7 | ||||
| chr4:82430402-82430825 | Common:3; Rare:153 | ||||
| chr4:82561967-82562078 | Rare:28 | ||||
| chr4:82890990-82891309 | Common:1; Rare:120 | ||||
| chr4:82900333-82900831 | Common:1; Rare:143 | ||||
| chr4:82900872-82901154 | Common:1; Rare:120 | ||||
| chr4:83012796-83013185 | Common:1; Rare:111 | ||||
| chr4:83284534-83284855 | Common:2; Rare:142; Clinvar:6; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr4:83334801-83334992 | Rare:46 | ||||
| chr4:83455759-83456165 | Common:3; Rare:160 | ||||
| chr4:83485065-83485287 | Common:3; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:83535681-83535743 | Rare:14 | ||||
| chr4:83535776-83536535 | Common:3; Rare:206 | ||||
| chr4:84966651-84966737 | Rare:21 | ||||
| chr4:86594055-86594350 | Rare:94 |