| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:32474924-32475059 | Rare:52 | ||||
| chr22:35257410-35257513 | Common:1; Rare:28 | ||||
| chr22:35299738-35299979 | Common:2; Rare:66 | ||||
| chr22:35300275-35300320 | Rare:15 | ||||
| chr22:35322857-35323087 | Rare:76 | ||||
| chr22:35399905-35400208 | Rare:106 | ||||
| chr22:36252990-36253194 | Rare:41 | ||||
| chr22:36285656-36285962 | Rare:114; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:36319539-36319712 | Rare:46; Clinvar (benign):3 | ||||
| chr22:36387812-36388330 | Common:2; Rare:133; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:36481548-36481668 | Common:1; Rare:40 | ||||
| chr22:36507024-36507173 | Common:3; Rare:50 | ||||
| chr22:36529074-36529544 | Common:6; Rare:148 | ||||
| chr22:37019404-37019778 | Common:5; Rare:107 | ||||
| chr22:37560331-37560581 | Common:1; Rare:86 |