| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144428480-144428676 | Common:2; Rare:77 | ||||
| chr8:144477892-144478080 | Common:4; Rare:73 | ||||
| chr8:144755461-144755663 | Common:1; Rare:67 | ||||
| chr8:144792356-144792562 | Common:2; Rare:75 | ||||
| chr9:2015077-2015387 | Common:3; Rare:89 | ||||
| chr9:2844049-2844341 | Common:5; Rare:108 | ||||
| chr9:4679445-4679715 | Common:1; Rare:116 | ||||
| chr9:5437809-5437982 | Common:1; Rare:62 | ||||
| chr9:6015610-6015772 | Rare:71 | ||||
| chr9:13279616-13279811 | Common:2; Rare:61 | ||||
| chr9:15422580-15422896 | Common:1; Rare:140 | ||||
| chr9:19380191-19380397 | Common:5; Rare:100 | ||||
| chr9:20684113-20684283 | Common:2; Rare:64 | ||||
| chr9:21802548-21802668 | Rare:29; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21975123-21975321 | Common:2; Rare:49; Clinvar (benign):1 |