| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20858684-20859044 | Common:5; Rare:171; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:20982196-20982322 | Common:2; Rare:26; Clinvar (benign):2 | ||||
| chr22:21002106-21002251 | Common:4; Rare:48 | ||||
| chr22:21982759-21982892 | Rare:32 | ||||
| chr22:23579995-23580084 | Rare:22 | ||||
| chr22:23580218-23580508 | Common:2; Rare:64 | ||||
| chr22:23696388-23696678 | Common:1; Rare:106 | ||||
| chr22:23754330-23754551 | Common:4; Rare:55 | ||||
| chr22:23767925-23768058 | Rare:35 | ||||
| chr22:23857572-23857933 | Common:7; Rare:153 | ||||
| chr22:23894252-23894795 | Common:6; Rare:203 | ||||
| chr22:24011041-24011335 | Common:42; Rare:161 | ||||
| chr22:24270694-24270911 | Common:3; Rare:86 | ||||
| chr22:24555903-24556071 | Rare:49 | ||||
| chr22:26483758-26483941 | Common:4; Rare:72; Clinvar:5; Clinvar (benign):1 |