| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46762440-46762669 | Common:3; Rare:89 | ||||
| chr22:49918273-49918631 | Common:4; Rare:112; Clinvar (benign):3 | ||||
| chr22:50185690-50185942 | Common:4; Rare:106 | ||||
| chr22:50244516-50244662 | Common:1; Rare:48 | ||||
| chr22:50244949-50245096 | Common:2; Rare:58 | ||||
| chr22:50525531-50525674 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50532145-50532310 | Common:1; Rare:42 | ||||
| chr22:50582790-50583121 | Common:7; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628082-50628276 | Common:9; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783601-50783859 | Common:2; Rare:79 | ||||
| chr3:196702-196908 | Common:1; Rare:66 | ||||
| chr3:197194-197334 | Rare:44 | ||||
| chr3:197345-197649 | Common:5; Rare:98 | ||||
| chr3:2098651-2098957 | Common:4; Rare:122 | ||||
| chr3:3126764-3127008 | Common:4; Rare:110; Clinvar (benign):4 |