| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:108728252-108728431 | Rare:62 | ||||
| chr5:109091442-109091634 | Common:1; Rare:38 | ||||
| chr5:109690020-109690137 | Common:1; Rare:32 | ||||
| chr5:109690318-109690510 | Rare:77 | ||||
| chr5:112160628-112161195 | Common:4; Rare:191 | ||||
| chr5:112419905-112420137 | Common:5; Rare:104 | ||||
| chr5:112780624-112780858 | Common:1; Rare:67; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr5:113027479-113027542 | Rare:24 | ||||
| chr5:116572867-116573050 | Common:3; Rare:59 | ||||
| chr5:118973740-118973918 | Common:3; Rare:41 | ||||
| chr5:119287202-119287358 | Common:6; Rare:26 | ||||
| chr5:119299689-119299976 | Common:5; Rare:78 | ||||
| chr5:119341742-119341964 | Common:1; Rare:49 | ||||
| chr5:123401590-123401905 | Common:3; Rare:56 | ||||
| chr5:124843357-124843511 | Common:1; Rare:30 |