| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41682286-41682851 | Common:10; Rare:544 | ||||
| chr22:41688602-41689432 | Common:14; Rare:872 | ||||
| chr22:41781105-41781550 | Common:6; Rare:220 | ||||
| chr22:41800100-41800786 | Common:14; Rare:575 | ||||
| chr22:41832556-41833348 | Common:18; Rare:855 | ||||
| chr22:41833517-41833968 | Common:6; Rare:206 | ||||
| chr22:41915000-41915370 | Common:8; Rare:94 | ||||
| chr22:41925910-41926470 | Common:8; Rare:294; Clinvar:12; Clinvar (benign):16 | ||||
| chr22:41946076-41946542 | Common:5; Rare:270 | ||||
| chr22:41946647-41947047 | Common:20; Rare:488 | ||||
| chr22:41947060-41947400 | Common:4; Rare:397 | ||||
| chr22:42069695-42071093 | Common:31; Rare:975; Clinvar:7; Clinvar (benign):2 | ||||
| chr22:42071100-42071470 | Common:1; Rare:96 | ||||
| chr22:42079058-42079786 | Common:20; Rare:591 | ||||
| chr22:42079875-42080172 | Rare:179 |