Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:93228228-93228340 | Common:1; Rare:33 | ||||
chr13:102394502-102394660 | Common:1; Rare:58 | ||||
chr13:108915757-108915891 | Rare:23 | ||||
chr13:109781685-109782015 | Common:5; Rare:80 | ||||
chr13:109785266-109785615 | Common:2; Rare:113 | ||||
chr13:110174444-110174713 | Rare:89; Clinvar (benign):3 | ||||
chr13:110205351-110205540 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:110250826-110250872 | Common:1; Rare:5 | ||||
chr13:110259370-110259514 | Rare:34 | ||||
chr13:110281187-110281388 | Common:1; Rare:34 | ||||
chr13:110304263-110304469 | Common:1; Rare:32 | ||||
chr13:110307856-110308123 | Common:1; Rare:101 | ||||
chr13:110308510-110308610 | Common:1; Rare:22 | ||||
chr13:110311817-110311919 | Rare:35 | ||||
chr13:110313933-110313984 | Rare:4 |