| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:22704005-22704009 | |||||
| chr22:25448001-25448153 | Common:4; Rare:58 | ||||
| chr22:26672877-26673104 | Common:1; Rare:68 | ||||
| chr22:28799138-28799420 | Rare:50 | ||||
| chr22:30969036-30969302 | Common:2; Rare:77 | ||||
| chr22:36288725-36289135 | Common:2; Rare:119; Clinvar:3; Clinvar (benign):6 | ||||
| chr22:37307976-37308064 | Common:2; Rare:23 | ||||
| chr22:46069855-46070105 | Rare:56 | ||||
| chr3:23947550-23947836 | Common:8; Rare:68 | ||||
| chr3:45224809-45224866 | Common:1; Rare:9 | ||||
| chr3:49026526-49026836 | Common:2; Rare:90; Clinvar:1 | ||||
| chr3:57952303-57952439 | Rare:22 | ||||
| chr3:62587291-62587504 | Common:2; Rare:42 | ||||
| chr3:75435017-75435395 | Common:5; Rare:130 | ||||
| chr3:81761480-81761614 | Common:5; Rare:49; Clinvar:1; Clinvar (benign):2 |