Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45455781-45455982 | Common:1; Rare:49 | ||||
chr19:45717285-45717540 | Common:1; Rare:69 | ||||
chr19:46860833-46861141 | Common:3; Rare:97 | ||||
chr19:48966280-48966729 | Rare:151; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr19:48969779-48969935 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49491460-49491736 | Common:2; Rare:79 | ||||
chr19:49640730-49640863 | Rare:17 | ||||
chr19:58550606-58550894 | Common:1; Rare:86 | ||||
chr2:38146937-38147217 | Common:1; Rare:68 | ||||
chr2:47335235-47335323 | Rare:19 | ||||
chr2:47798515-47798678 | Common:2; Rare:67; Clinvar:20; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
chr2:47906514-47906815 | Common:2; Rare:99 | ||||
chr2:61764225-61764519 | Common:4; Rare:100 | ||||
chr2:65436412-65436687 | Common:1; Rare:65 | ||||
chr2:66839930-66840369 | Common:1; Rare:79 |