| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31753749-31754107 | Common:1; Rare:128 | ||||
| chr22:32043038-32043433 | Common:3; Rare:127; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr22:32255331-32255423 | Rare:21 | ||||
| chr22:32412128-32412535 | Common:3; Rare:118 | ||||
| chr22:32474911-32475019 | Rare:39 | ||||
| chr22:35066025-35066764 | Common:4; Rare:133 | ||||
| chr22:35399915-35400183 | Rare:93 | ||||
| chr22:36285634-36286006 | Rare:128; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:36387992-36388333 | Common:1; Rare:92 | ||||
| chr22:36481566-36481729 | Common:2; Rare:45 | ||||
| chr22:36529086-36529483 | Common:5; Rare:120 | ||||
| chr22:37019395-37019839 | Common:5; Rare:132 | ||||
| chr22:37024102-37024311 | Common:1; Rare:58 | ||||
| chr22:37560331-37560549 | Common:1; Rare:75 | ||||
| chr22:37608665-37608881 | Common:2; Rare:67 |