| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:25339095-25339392 | Common:1; Rare:54 | ||||
| chr8:27902383-27902815 | Common:3; Rare:80 | ||||
| chr8:30091325-30091484 | Common:1; Rare:36 | ||||
| chr8:30385968-30386086 | Common:1; Rare:15 | ||||
| chr8:30427363-30427421 | Rare:10 | ||||
| chr8:30509380-30509413 | Common:1; Rare:1 | ||||
| chr8:37697016-37697309 | Common:2; Rare:88 | ||||
| chr8:37744264-37744380 | Rare:30; Clinvar (pathogenic):1 | ||||
| chr8:37748002-37748087 | Rare:38 | ||||
| chr8:38770169-38770221 | Rare:6 | ||||
| chr8:42649982-42650215 | Common:1; Rare:55 | ||||
| chr8:42666979-42667154 | Common:1; Rare:28 | ||||
| chr8:42861756-42862067 | Rare:58 | ||||
| chr8:47385622-47385750 | Rare:24 | ||||
| chr8:47512269-47512569 | Rare:63 |