| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:119452413-119452785 | Common:1; Rare:171; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:120464175-120464373 | Common:1; Rare:61 | ||||
| chr5:121961800-121962034 | Common:2; Rare:82 | ||||
| chr5:122774851-122775140 | Common:1; Rare:117 | ||||
| chr5:122845516-122845625 | Common:3; Rare:43 | ||||
| chr5:123036424-123036492 | Rare:26 | ||||
| chr5:123036615-123036981 | Common:2; Rare:92 | ||||
| chr5:123511954-123512268 | Common:1; Rare:93 | ||||
| chr5:124746284-124746581 | Common:2; Rare:51 | ||||
| chr5:124748753-124749004 | Common:2; Rare:55 | ||||
| chr5:126423359-126423618 | Rare:76 | ||||
| chr5:126595183-126595438 | Common:4; Rare:96; Clinvar:4; Clinvar (benign):9 | ||||
| chr5:126776902-126777175 | Common:1; Rare:109; Clinvar:4; Clinvar (benign):3 | ||||
| chr5:127030509-127030704 | Common:2; Rare:46 | ||||
| chr5:127290651-127290852 | Rare:43 |