| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:26382945-26383110 | Rare:74 | ||||
| chr8:30156250-30156373 | Rare:32 | ||||
| chr8:33485001-33485186 | Common:3; Rare:66 | ||||
| chr8:38176677-38176860 | Common:2; Rare:47 | ||||
| chr8:38996452-38996958 | Common:5; Rare:170 | ||||
| chr8:42541557-42541683 | Rare:45 | ||||
| chr8:42541691-42541837 | Rare:56 | ||||
| chr8:47260774-47260983 | Common:3; Rare:94 | ||||
| chr8:47960133-47960255 | Common:1; Rare:36; Clinvar (benign):1 | ||||
| chr8:56074388-56074592 | Common:3; Rare:102 | ||||
| chr8:60516771-60517106 | Common:3; Rare:118 | ||||
| chr8:63168454-63168659 | Common:1; Rare:68 | ||||
| chr8:63168923-63169022 | Rare:46 | ||||
| chr8:67061991-67062236 | Common:1; Rare:81 | ||||
| chr8:70608206-70608502 | Common:3; Rare:92 |