| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:1755561-1755944 | Common:5; Rare:117 | ||||
| chr8:1823721-1824093 | Common:10; Rare:142 | ||||
| chr8:6406526-6406680 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr8:6562691-6562917 | Common:1; Rare:80 | ||||
| chr8:6708142-6708422 | Common:3; Rare:125 | ||||
| chr8:6708485-6708645 | Common:1; Rare:64 | ||||
| chr8:6835450-6835576 | Rare:53 | ||||
| chr8:9151611-9151776 | Common:1; Rare:59 | ||||
| chr8:10839783-10839999 | Rare:87 | ||||
| chr8:11201801-11201889 | Rare:22 | ||||
| chr8:11284728-11284848 | Common:2; Rare:50 | ||||
| chr8:11769565-11769818 | Common:5; Rare:111 | ||||
| chr8:11802443-11802818 | Common:6; Rare:201 | ||||
| chr8:11847686-11848100 | Common:7; Rare:228; Clinvar (benign):1 | ||||
| chr8:13514859-13514898 | Rare:9 |