| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:26382960-26383090 | Rare:55 | ||||
| chr8:27311273-27311548 | Common:6; Rare:93 | ||||
| chr8:27772570-27772752 | Common:6; Rare:60 | ||||
| chr8:30156268-30156373 | Rare:24 | ||||
| chr8:33485022-33485204 | Common:2; Rare:61 | ||||
| chr8:37762507-37762642 | Common:1; Rare:47 | ||||
| chr8:38176455-38176872 | Common:5; Rare:114 | ||||
| chr8:38269195-38269257 | Rare:18 | ||||
| chr8:41490348-41490613 | Rare:61 | ||||
| chr8:42541558-42541666 | Rare:36 | ||||
| chr8:42541688-42541917 | Common:1; Rare:74; Clinvar (benign):1 | ||||
| chr8:43093345-43093545 | Common:2; Rare:40 | ||||
| chr8:47960693-47960993 | Common:2; Rare:110; Clinvar:9; Clinvar (benign):1 | ||||
| chr8:52714427-52714526 | Common:1; Rare:39 | ||||
| chr8:55773371-55773496 | Common:3; Rare:42 |