| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:42541911-42542296 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:42843273-42843511 | Common:2; Rare:68; Clinvar (benign):3 | ||||
| chr8:42896288-42896382 | Rare:38 | ||||
| chr8:42896591-42897052 | Common:1; Rare:183 | ||||
| chr8:42897279-42897426 | Common:1; Rare:42 | ||||
| chr8:43056132-43056460 | Common:1; Rare:119 | ||||
| chr8:43140241-43140582 | Common:3; Rare:131; Clinvar:9 | ||||
| chr8:47260700-47260981 | Common:3; Rare:120 | ||||
| chr8:47960068-47960191 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960811-47960974 | Common:1; Rare:65; Clinvar:6 | ||||
| chr8:51898951-51899331 | Common:7; Rare:169 | ||||
| chr8:51899511-51899670 | Rare:31 | ||||
| chr8:52565326-52565574 | Rare:71 | ||||
| chr8:52714077-52714613 | Common:2; Rare:199 | ||||
| chr8:53843207-53843354 | Rare:35 |