| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17628652-17628887 | Common:3; Rare:169 | ||||
| chr22:17638294-17639041 | Common:3; Rare:274 | ||||
| chr22:17773836-17774236 | Common:5; Rare:183 | ||||
| chr22:17774301-17774925 | Common:3; Rare:197 | ||||
| chr22:18001412-18001551 | Common:2; Rare:54 | ||||
| chr22:18077769-18078062 | Common:11; Rare:165; Clinvar:6; Clinvar (benign):5 | ||||
| chr22:18149666-18150198 | Common:4; Rare:212 | ||||
| chr22:19122283-19122900 | Common:13; Rare:233 | ||||
| chr22:19144626-19144874 | Common:8; Rare:158 | ||||
| chr22:19178235-19178528 | Common:4; Rare:133; Clinvar (benign):4 | ||||
| chr22:19178606-19179053 | Common:8; Rare:288; Clinvar (benign):4 | ||||
| chr22:19291654-19291977 | Common:24; Rare:220 | ||||
| chr22:19431227-19431358 | Rare:64 | ||||
| chr22:19431664-19431838 | Rare:88 | ||||
| chr22:19432273-19432614 | Common:8; Rare:284 |