| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:112707327-112707611 | Common:8; Rare:121; Clinvar:64; Clinvar (benign):14; Clinvar (pathogenic):1 | ||||
| chr5:112976503-112976851 | Common:2; Rare:158 | ||||
| chr5:113513658-113513714 | Rare:18 | ||||
| chr5:115262819-115262927 | Common:1; Rare:52 | ||||
| chr5:115544648-115545024 | Common:2; Rare:141 | ||||
| chr5:115841524-115842099 | Common:7; Rare:240 | ||||
| chr5:116085371-116085462 | Rare:21 | ||||
| chr5:119268573-119268837 | Common:1; Rare:72 | ||||
| chr5:119355798-119356021 | Common:2; Rare:61 | ||||
| chr5:121961849-121962040 | Common:2; Rare:67 | ||||
| chr5:122774905-122775135 | Rare:94 | ||||
| chr5:122845516-122845636 | Common:3; Rare:47 | ||||
| chr5:123036636-123036817 | Common:2; Rare:53 | ||||
| chr5:123423317-123423597 | Rare:93 | ||||
| chr5:126423318-126423493 | Rare:45 |