| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112737722-112737908 | Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:112861201-112861378 | Common:3; Rare:73 | ||||
| chr5:112976445-112976865 | Common:3; Rare:189 | ||||
| chr5:113513645-113513714 | Rare:21 | ||||
| chr5:115626167-115626224 | Rare:7 | ||||
| chr5:115816654-115816761 | Rare:19 | ||||
| chr5:115841481-115841589 | Common:2; Rare:75 | ||||
| chr5:115841818-115842058 | Common:4; Rare:77 | ||||
| chr5:116574203-116574366 | Rare:51 | ||||
| chr5:116574469-116574646 | Common:3; Rare:42 | ||||
| chr5:116574820-116574948 | Common:2; Rare:42 | ||||
| chr5:116575013-116575141 | Common:1; Rare:29 | ||||
| chr5:119268579-119268804 | Common:1; Rare:65 | ||||
| chr5:121961941-121962066 | Common:1; Rare:60 | ||||
| chr5:122774859-122775133 | Common:1; Rare:111 |