| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:47737307-47737380 | Common:1; Rare:29 | ||||
| chr8:72052751-72052824 | Common:1; Rare:18 | ||||
| chr8:73063073-73063143 | Common:1; Rare:16 | ||||
| chr8:73063208-73063312 | Common:3; Rare:14 | ||||
| chr8:103329460-103329842 | Common:2; Rare:82 | ||||
| chr8:107497269-107497344 | Common:1; Rare:18 | ||||
| chr8:117913704-117913975 | Common:3; Rare:48 | ||||
| chr8:117989535-117989840 | Rare:50 | ||||
| chr8:118924657-118925045 | Common:3; Rare:94; Clinvar (benign):1 | ||||
| chr8:123512427-123512497 | Rare:9 | ||||
| chr8:123518261-123518381 | Rare:16 | ||||
| chr8:125951148-125951328 | Common:2; Rare:27 | ||||
| chr8:133072167-133072369 | Common:2; Rare:38 | ||||
| chr8:143816781-143816988 | Common:1; Rare:69 | ||||
| chr8:143927675-143927885 | Common:3; Rare:88; Clinvar:12; Clinvar (benign):3 |