| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:35257610-35257921 | Rare:99 | ||||
| chr22:35299587-35299914 | Common:3; Rare:83 | ||||
| chr22:35399891-35400226 | Rare:121 | ||||
| chr22:36387927-36388322 | Common:2; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481304-36481399 | Common:1; Rare:16 | ||||
| chr22:36481558-36481729 | Common:2; Rare:46 | ||||
| chr22:36482002-36482236 | Common:1; Rare:60 | ||||
| chr22:36507081-36507212 | Common:3; Rare:59 | ||||
| chr22:36528884-36528987 | Rare:41 | ||||
| chr22:36529057-36529567 | Common:8; Rare:158 | ||||
| chr22:36776065-36776361 | Common:2; Rare:69 | ||||
| chr22:37199383-37199654 | Common:4; Rare:71 | ||||
| chr22:37608435-37608496 | Common:1; Rare:28 | ||||
| chr22:37608679-37609064 | Common:2; Rare:113 | ||||
| chr22:37633886-37634186 | Rare:70 |