| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:115544648-115545052 | Common:2; Rare:153 | ||||
| chr5:115841484-115841614 | Common:2; Rare:82 | ||||
| chr5:115841831-115842105 | Common:4; Rare:87 | ||||
| chr5:119268631-119268837 | Common:1; Rare:58 | ||||
| chr5:119355825-119356022 | Common:2; Rare:50 | ||||
| chr5:121961710-121962062 | Common:15; Rare:133 | ||||
| chr5:122845516-122845621 | Common:3; Rare:40 | ||||
| chr5:123036657-123037020 | Common:2; Rare:92 | ||||
| chr5:123423336-123423422 | Rare:37 | ||||
| chr5:126423374-126423594 | Rare:66 | ||||
| chr5:126595132-126595327 | Common:3; Rare:92; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr5:127030537-127030678 | Common:1; Rare:34 | ||||
| chr5:127517502-127517699 | Common:6; Rare:89 | ||||
| chr5:131170792-131171002 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr5:131252949-131253071 | Common:1; Rare:26 |