| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801246-121801445 | Common:2; Rare:66 | ||||
| chr4:121823858-121824007 | Common:1; Rare:43 | ||||
| chr4:121870406-121870669 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr4:122152257-122152423 | Common:2; Rare:70 | ||||
| chr4:122309059-122309460 | Rare:70 | ||||
| chr4:122378735-122379115 | Common:1; Rare:85 | ||||
| chr4:122379319-122379610 | Common:1; Rare:101 | ||||
| chr4:122732400-122732791 | Common:4; Rare:126; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922400-122922585 | Common:2; Rare:97 | ||||
| chr4:122922588-122922672 | Rare:32 | ||||
| chr4:122922933-122923147 | Common:2; Rare:69; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396756-123396827 | Rare:24 | ||||
| chr4:123398344-123398469 | Common:1; Rare:43 | ||||
| chr4:124712579-124713063 | Common:1; Rare:138 | ||||
| chr4:127622948-127623285 | Common:1; Rare:77 |