| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:98773435-98773703 | Common:7; Rare:72 | ||||
| chr5:98773819-98774067 | Common:2; Rare:85 | ||||
| chr5:98928881-98929197 | Common:4; Rare:132 | ||||
| chr5:100535232-100535399 | Rare:40 | ||||
| chr5:100903213-100903394 | Rare:35 | ||||
| chr5:102755129-102755339 | Common:1; Rare:75 | ||||
| chr5:103120106-103120404 | Common:1; Rare:71 | ||||
| chr5:108380943-108381217 | Common:2; Rare:81 | ||||
| chr5:108382061-108382147 | Common:1; Rare:30 | ||||
| chr5:108748673-108748991 | Common:2; Rare:110 | ||||
| chr5:109409835-109410225 | Common:4; Rare:148 | ||||
| chr5:109689827-109689952 | Common:1; Rare:46 | ||||
| chr5:110738919-110739088 | Common:2; Rare:68 | ||||
| chr5:112419187-112419293 | Common:1; Rare:48 | ||||
| chr5:112707753-112707840 | Rare:32; Clinvar:15; Clinvar (benign):1 |