Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10652311-10652505 | Common:1; Rare:35 | ||||
chr19:10675774-10675902 | Rare:36 | ||||
chr19:11036761-11036901 | Common:1; Rare:26 | ||||
chr19:11178381-11178628 | Common:2; Rare:94 | ||||
chr19:11204080-11204271 | Common:3; Rare:60 | ||||
chr19:11437948-11438138 | Common:1; Rare:65; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:12661365-12661452 | Common:1; Rare:17 | ||||
chr19:12793233-12793309 | Common:1; Rare:18 | ||||
chr19:12891963-12892157 | Rare:64; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
chr19:12944457-12944559 | Common:3; Rare:36 | ||||
chr19:13088274-13088475 | Rare:46 | ||||
chr19:13110656-13110720 | Rare:13 | ||||
chr19:13167585-13167692 | Rare:31 | ||||
chr19:13796560-13796578 | Rare:4 | ||||
chr19:13827334-13827546 | Common:3; Rare:42 |