| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50185690-50185960 | Common:4; Rare:112 | ||||
| chr22:50190422-50190637 | Common:3; Rare:66 | ||||
| chr22:50192927-50193061 | Rare:36 | ||||
| chr22:50244941-50245070 | Common:2; Rare:47 | ||||
| chr22:50283126-50283304 | Common:1; Rare:53 | ||||
| chr22:50286077-50286217 | Common:1; Rare:45 | ||||
| chr22:50455365-50455510 | Common:1; Rare:49; Clinvar (pathogenic):1 | ||||
| chr22:50505763-50506073 | Common:5; Rare:154 | ||||
| chr22:50525524-50525706 | Common:4; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50530931-50531193 | Rare:88 | ||||
| chr22:50532124-50532223 | Rare:24 | ||||
| chr22:50532471-50532665 | Common:2; Rare:46 | ||||
| chr22:50562887-50563059 | Common:3; Rare:46 | ||||
| chr22:50582790-50583120 | Common:7; Rare:101; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50628000-50628276 | Common:9; Rare:118; Clinvar:4; Clinvar (benign):1 |