| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:82044250-82044640 | Common:4; Rare:179 | ||||
| chr4:82372960-82373640 | Common:3; Rare:552 | ||||
| chr4:82373681-82374555 | Common:11; Rare:608 | ||||
| chr4:82429284-82429743 | Common:4; Rare:599; Clinvar:40; Clinvar (benign):21 | ||||
| chr4:82429812-82430833 | Common:12; Rare:795 | ||||
| chr4:82561820-82562316 | Common:3; Rare:319 | ||||
| chr4:82798725-82799012 | Common:11; Rare:179 | ||||
| chr4:82890821-82891514 | Common:8; Rare:446 | ||||
| chr4:82900325-82900840 | Common:2; Rare:322 | ||||
| chr4:82900788-82901240 | Common:3; Rare:367 | ||||
| chr4:83010704-83010985 | Rare:87 | ||||
| chr4:83012795-83013418 | Common:8; Rare:396 | ||||
| chr4:83034616-83035257 | Common:7; Rare:335 | ||||
| chr4:83109750-83110120 | Common:4; Rare:175 | ||||
| chr4:83284300-83284877 | Common:6; Rare:360; Clinvar:12; Clinvar (benign):13; Clinvar (pathogenic):5 |