| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111757170-111757342 | Common:5; Rare:34 | ||||
| chr5:112861108-112861396 | Common:5; Rare:113 | ||||
| chr5:112976457-112976882 | Common:3; Rare:197 | ||||
| chr5:113294647-113294726 | Rare:20 | ||||
| chr5:115262829-115262927 | Rare:47 | ||||
| chr5:115841490-115842081 | Common:8; Rare:254 | ||||
| chr5:119268579-119268821 | Common:1; Rare:69 | ||||
| chr5:122845484-122845621 | Common:3; Rare:53 | ||||
| chr5:123036624-123037027 | Common:2; Rare:104 | ||||
| chr5:126776844-126777203 | Common:3; Rare:135; Clinvar:4; Clinvar (benign):6 | ||||
| chr5:128082982-128083372 | Common:8; Rare:120 | ||||
| chr5:131170670-131171008 | Common:1; Rare:79; Clinvar (benign):2 | ||||
| chr5:131635163-131635422 | Common:1; Rare:96 | ||||
| chr5:131796969-131797206 | Rare:66 | ||||
| chr5:132257496-132257737 | Common:8; Rare:59 |