| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108748686-108748982 | Common:2; Rare:98 | ||||
| chr5:109689249-109689448 | Common:4; Rare:95 | ||||
| chr5:109689807-109689966 | Common:1; Rare:56 | ||||
| chr5:109804030-109804198 | Common:1; Rare:31 | ||||
| chr5:110738929-110739141 | Common:2; Rare:93; Clinvar (pathogenic):1 | ||||
| chr5:110739331-110739335 | Rare:2 | ||||
| chr5:112419192-112419287 | Common:1; Rare:41 | ||||
| chr5:112861108-112861368 | Common:4; Rare:100 | ||||
| chr5:112976503-112976840 | Common:2; Rare:149 | ||||
| chr5:113203257-113203413 | Common:2; Rare:42 | ||||
| chr5:113204586-113204771 | Rare:36 | ||||
| chr5:113294629-113294860 | Common:1; Rare:56 | ||||
| chr5:113513624-113513924 | Common:1; Rare:102 | ||||
| chr5:115262837-115262888 | Rare:25 | ||||
| chr5:115544733-115545026 | Common:2; Rare:120 |