| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:109689835-109689947 | Common:1; Rare:41 | ||||
| chr5:110738930-110739124 | Common:2; Rare:84 | ||||
| chr5:111757620-111757815 | Common:1; Rare:80 | ||||
| chr5:112419192-112419309 | Common:1; Rare:49 | ||||
| chr5:112861190-112861378 | Common:3; Rare:76 | ||||
| chr5:112976503-112976888 | Common:3; Rare:182 | ||||
| chr5:113294595-113294711 | Rare:39 | ||||
| chr5:115262829-115262883 | Rare:26 | ||||
| chr5:115841490-115842046 | Common:8; Rare:246 | ||||
| chr5:116084896-116085055 | Common:7; Rare:67 | ||||
| chr5:119268625-119268821 | Common:1; Rare:57 | ||||
| chr5:121961850-121962032 | Common:2; Rare:66 | ||||
| chr5:122077101-122077236 | Common:1; Rare:21 | ||||
| chr5:123512060-123512273 | Rare:59 | ||||
| chr5:126776844-126777184 | Common:3; Rare:129; Clinvar:4; Clinvar (benign):5 |