| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119452339-119452572 | Common:1; Rare:81; Clinvar (benign):4 | ||||
| chr5:120464053-120464453 | Common:2; Rare:134 | ||||
| chr5:121961604-121962040 | Common:16; Rare:145 | ||||
| chr5:122078286-122078473 | Common:1; Rare:44 | ||||
| chr5:122129458-122129581 | Common:1; Rare:34 | ||||
| chr5:122311565-122311769 | Common:3; Rare:35 | ||||
| chr5:122312052-122312237 | Rare:59 | ||||
| chr5:122312280-122312710 | Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:122313043-122313171 | Common:1; Rare:29 | ||||
| chr5:122774851-122775179 | Common:1; Rare:134 | ||||
| chr5:122845313-122845616 | Common:3; Rare:101 | ||||
| chr5:123036450-123036910 | Common:2; Rare:135 | ||||
| chr5:123423192-123423618 | Common:1; Rare:134 | ||||
| chr5:123511884-123512362 | Common:3; Rare:149 | ||||
| chr5:124745830-124746230 | Common:2; Rare:97 |