| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:2127501-2127805 | Common:14; Rare:75 | ||||
| chr8:6406527-6406671 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6708162-6708347 | Common:2; Rare:70 | ||||
| chr8:6709068-6709215 | Common:2; Rare:60 | ||||
| chr8:10839815-10840146 | Common:3; Rare:111 | ||||
| chr8:11200785-11200859 | Rare:30 | ||||
| chr8:11201801-11201961 | Common:1; Rare:48 | ||||
| chr8:11493826-11494234 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):3 | ||||
| chr8:11494314-11494507 | Common:1; Rare:56; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:11545709-11545944 | Common:1; Rare:70 | ||||
| chr8:11546000-11546094 | Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:11560061-11560267 | Common:13; Rare:34 | ||||
| chr8:11769565-11769913 | Common:5; Rare:142 | ||||
| chr8:11802443-11802920 | Common:7; Rare:258 | ||||
| chr8:11802924-11803033 | Rare:68 |