| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:31033566-31033844 | Common:3; Rare:67; Clinvar:4; Clinvar (benign):3 | ||||
| chr8:33484993-33485193 | Common:4; Rare:69 | ||||
| chr8:37796567-37796908 | Rare:99 | ||||
| chr8:38105358-38105561 | Common:2; Rare:61 | ||||
| chr8:38105775-38105930 | Rare:46 | ||||
| chr8:38176434-38176863 | Common:5; Rare:118 | ||||
| chr8:38757191-38757309 | Common:1; Rare:25 | ||||
| chr8:38996266-38996299 | Common:1; Rare:20 | ||||
| chr8:38996459-38997003 | Common:7; Rare:194 | ||||
| chr8:42051976-42052115 | Rare:40 | ||||
| chr8:42541494-42541661 | Common:2; Rare:45 | ||||
| chr8:42541673-42541854 | Rare:67 | ||||
| chr8:42896562-42897007 | Common:1; Rare:183 | ||||
| chr8:43093425-43093547 | Common:2; Rare:25 | ||||
| chr8:47260771-47260989 | Common:3; Rare:99 |