| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19941577-19941643 | Common:1; Rare:17 | ||||
| chr22:19941730-19941971 | Rare:90; Clinvar:4; Clinvar (benign):4 | ||||
| chr22:19942371-19942597 | Common:5; Rare:45 | ||||
| chr22:20020711-20020731 | Rare:3 | ||||
| chr22:20020792-20021211 | Common:2; Rare:125 | ||||
| chr22:20079813-20080314 | Common:1; Rare:160 | ||||
| chr22:20116941-20117598 | Common:4; Rare:193 | ||||
| chr22:20117949-20118111 | Rare:45 | ||||
| chr22:20131018-20131321 | Common:5; Rare:105 | ||||
| chr22:20131685-20131845 | Common:2; Rare:42 | ||||
| chr22:20243647-20243836 | Rare:35 | ||||
| chr22:20319956-20320272 | Common:2; Rare:111 | ||||
| chr22:20372680-20372752 | Common:1; Rare:8 | ||||
| chr22:20393883-20394242 | Common:2; Rare:101 | ||||
| chr22:20495739-20496136 | Common:3; Rare:127 |