| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:23000710-23001040 | Rare:48 | ||||
| chr8:23336030-23336470 | Common:2; Rare:83 | ||||
| chr8:23861894-23862294 | Common:3; Rare:80 | ||||
| chr8:24039260-24039620 | Common:5; Rare:74 | ||||
| chr8:24045918-24046472 | Common:10; Rare:182 | ||||
| chr8:24567560-24567890 | Common:1; Rare:64 | ||||
| chr8:24612014-24612990 | Common:7; Rare:219 | ||||
| chr8:24726690-24727090 | Common:5; Rare:96 | ||||
| chr8:24766450-24766860 | Common:1; Rare:70 | ||||
| chr8:24768099-24768499 | Common:8; Rare:108 | ||||
| chr8:24941840-24942200 | Common:2; Rare:68 | ||||
| chr8:24955016-24955776 | Common:4; Rare:381; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr8:24958620-24959020 | Common:17; Rare:78 | ||||
| chr8:25000032-25000250 | Common:1; Rare:48 | ||||
| chr8:25000349-25000517 | Common:1; Rare:31 |