| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46267868-46268048 | Common:1; Rare:59 | ||||
| chr22:46335621-46335760 | Common:2; Rare:57; Clinvar:4; Clinvar (benign):6 | ||||
| chr22:46762506-46762706 | Common:3; Rare:74 | ||||
| chr22:49853601-49853925 | Common:2; Rare:115 | ||||
| chr22:49918408-49918680 | Common:1; Rare:96 | ||||
| chr22:50185723-50185942 | Common:4; Rare:92 | ||||
| chr22:50244960-50245113 | Common:2; Rare:61 | ||||
| chr22:50525543-50525706 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50532145-50532414 | Common:2; Rare:60 | ||||
| chr22:50582788-50583137 | Common:7; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628083-50628282 | Common:9; Rare:100; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783606-50783862 | Common:2; Rare:75 | ||||
| chr3:196706-196902 | Common:1; Rare:62 | ||||
| chr3:197186-197332 | Rare:48 | ||||
| chr3:197345-197666 | Common:6; Rare:105 |