| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23894281-23894544 | Common:3; Rare:96 | ||||
| chr22:23894576-23894903 | Common:3; Rare:132; Clinvar:1 | ||||
| chr22:24555843-24556068 | Rare:69 | ||||
| chr22:26483763-26483947 | Common:4; Rare:72; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512422-26512550 | Common:1; Rare:56 | ||||
| chr22:27919195-27919504 | Common:5; Rare:139 | ||||
| chr22:28741800-28742068 | Common:2; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:28742412-28742701 | Common:1; Rare:69 | ||||
| chr22:28800395-28800694 | Common:5; Rare:110 | ||||
| chr22:29267955-29268334 | Common:2; Rare:110 | ||||
| chr22:29553687-29553983 | Common:3; Rare:102 | ||||
| chr22:29767057-29767401 | Common:4; Rare:108 | ||||
| chr22:30326874-30327174 | Common:2; Rare:106 | ||||
| chr22:30356873-30357010 | Common:1; Rare:45 | ||||
| chr22:30607027-30607196 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):3 |