| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20606181-20606581 | Common:21; Rare:223 | ||||
| chr22:20702585-20702990 | Common:9; Rare:247 | ||||
| chr22:20885370-20885780 | Common:3; Rare:146 | ||||
| chr22:20885770-20886120 | Common:3; Rare:79 | ||||
| chr22:20887395-20887980 | Common:12; Rare:311; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr22:20920730-20921240 | Common:9; Rare:181 | ||||
| chr22:20957514-20957693 | Common:1; Rare:38 | ||||
| chr22:21002981-21003122 | Rare:71 | ||||
| chr22:21102951-21103067 | Rare:26 | ||||
| chr22:21657412-21657888 | Common:16; Rare:326 | ||||
| chr22:21657910-21658400 | Common:5; Rare:166 | ||||
| chr22:21684002-21684907 | Common:7; Rare:292 | ||||
| chr22:21807432-21807990 | Common:4; Rare:336 | ||||
| chr22:22297940-22298194 | Common:27; Rare:228 | ||||
| chr22:22925640-22926270 | Common:3; Rare:133 |