| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:111512438-111512760 | Common:3; Rare:116 | ||||
| chr5:111757152-111757335 | Common:5; Rare:37 | ||||
| chr5:112737797-112737895 | Rare:21; Clinvar (benign):1 | ||||
| chr5:112921548-112921854 | Common:4; Rare:90 | ||||
| chr5:112976520-112976859 | Common:2; Rare:156 | ||||
| chr5:113294625-113294689 | Rare:16 | ||||
| chr5:115262829-115262889 | Rare:29 | ||||
| chr5:115544728-115545030 | Common:2; Rare:122 | ||||
| chr5:115816655-115816831 | Common:1; Rare:44 | ||||
| chr5:115841516-115841625 | Common:1; Rare:72 | ||||
| chr5:115841791-115842024 | Common:3; Rare:77 | ||||
| chr5:119268590-119268811 | Common:1; Rare:64 | ||||
| chr5:119355825-119356021 | Common:2; Rare:50 | ||||
| chr5:120464113-120464373 | Common:1; Rare:73 | ||||
| chr5:122077091-122077288 | Common:1; Rare:35 |