Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:39214500-39214820 | Common:1; Rare:66 | ||||
chr22:39243970-39244044 | Rare:26 | ||||
chr22:39664986-39665095 | Rare:29 | ||||
chr22:40194038-40194272 | Rare:48 | ||||
chr22:40212740-40212932 | Common:1; Rare:41 | ||||
chr22:40361279-40361401 | Rare:30; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr22:40684894-40685030 | Rare:36 | ||||
chr22:41092434-41092624 | Rare:91 | ||||
chr22:41169323-41169616 | Common:1; Rare:87; Clinvar:1 | ||||
chr22:41197428-41197634 | Common:2; Rare:52 | ||||
chr22:41325589-41325778 | Rare:50 | ||||
chr22:41413940-41414043 | Rare:32 | ||||
chr22:41448524-41448775 | Common:3; Rare:61 | ||||
chr22:41694694-41694959 | Rare:40 | ||||
chr22:41695736-41695808 | Rare:11 |