| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40651724-40651905 | Common:3; Rare:52 | ||||
| chr22:40652116-40652279 | Rare:36 | ||||
| chr22:41092478-41092732 | Rare:107 | ||||
| chr22:41151665-41152009 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:41169368-41169625 | Common:1; Rare:73; Clinvar:1 | ||||
| chr22:41170239-41170570 | Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:41191878-41191988 | Rare:20 | ||||
| chr22:41197414-41197634 | Common:2; Rare:55 | ||||
| chr22:41413753-41414083 | Common:2; Rare:101 | ||||
| chr22:41444380-41444685 | Common:4; Rare:76 | ||||
| chr22:41532115-41532227 | Rare:51 | ||||
| chr22:41694079-41694429 | Common:1; Rare:58 | ||||
| chr22:41828668-41828808 | Common:2; Rare:26 | ||||
| chr22:41952030-41952125 | Common:2; Rare:18 | ||||
| chr22:42001914-42001996 | Rare:13 |