| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:30156243-30156395 | Rare:45 | ||||
| chr8:30744145-30744198 | Common:1; Rare:25 | ||||
| chr8:33484963-33485209 | Common:7; Rare:88 | ||||
| chr8:37695953-37696011 | Rare:15 | ||||
| chr8:37736489-37736753 | Common:3; Rare:90 | ||||
| chr8:38105356-38105548 | Common:2; Rare:57 | ||||
| chr8:38176426-38176596 | Common:1; Rare:56 | ||||
| chr8:38176674-38176881 | Common:4; Rare:59 | ||||
| chr8:38996462-38996789 | Common:4; Rare:103 | ||||
| chr8:42541554-42541759 | Rare:71 | ||||
| chr8:42843277-42843469 | Common:2; Rare:50; Clinvar (benign):3 | ||||
| chr8:42896516-42897049 | Common:1; Rare:208 | ||||
| chr8:47260787-47260981 | Common:3; Rare:84 | ||||
| chr8:47960011-47960230 | Common:1; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
| chr8:47960805-47961000 | Common:1; Rare:76; Clinvar:6 |