Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:11384193-11384431 | Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
chr19:11435094-11435720 | Common:7; Rare:193; Clinvar:2; Clinvar (benign):5 | ||||
chr19:11529073-11529256 | Rare:34 | ||||
chr19:11538588-11538865 | Common:2; Rare:59 | ||||
chr19:11559190-11559451 | Common:3; Rare:81 | ||||
chr19:11597295-11597520 | Common:1; Rare:66 | ||||
chr19:11738895-11739102 | Common:4; Rare:64 | ||||
chr19:11887668-11887906 | Common:1; Rare:75 | ||||
chr19:11924977-11925273 | Common:5; Rare:104 | ||||
chr19:11964906-11965082 | Common:1; Rare:46 | ||||
chr19:12052907-12053098 | Rare:49 | ||||
chr19:12064521-12064793 | Common:4; Rare:72 | ||||
chr19:12091988-12092358 | Common:2; Rare:88 | ||||
chr19:12140327-12140591 | Rare:68 | ||||
chr19:12156620-12156865 | Common:1; Rare:58 |