| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42179839-42180040 | Common:1; Rare:46 | ||||
| chr22:42211140-42211299 | Rare:58 | ||||
| chr22:42365536-42365672 | Rare:24 | ||||
| chr22:42496521-42496648 | Common:1; Rare:24 | ||||
| chr22:42580921-42581093 | Common:1; Rare:39 | ||||
| chr22:42581826-42582110 | Common:8; Rare:117 | ||||
| chr22:42596012-42596166 | Common:2; Rare:42 | ||||
| chr22:42623790-42624032 | Rare:79; Clinvar (pathogenic):1 | ||||
| chr22:42630880-42631224 | Common:3; Rare:92; Clinvar (pathogenic):1 | ||||
| chr22:42787709-42787942 | Common:2; Rare:45 | ||||
| chr22:43038476-43038600 | Rare:31 | ||||
| chr22:43039950-43040050 | Common:1; Rare:21 | ||||
| chr22:43187658-43187779 | Common:2; Rare:34 | ||||
| chr22:43205156-43205355 | Common:3; Rare:38 | ||||
| chr22:43321038-43321152 | Common:3; Rare:54 |