Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48966400-48966649 | Rare:75; Clinvar:1 | ||||
chr19:49104119-49104373 | Rare:66 | ||||
chr19:49491484-49491736 | Common:1; Rare:79 | ||||
chr19:49829858-49830092 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):4 | ||||
chr19:50724820-50725169 | Common:1; Rare:125 | ||||
chr19:51354775-51354990 | Common:1; Rare:34 | ||||
chr19:51594374-51594594 | Common:2; Rare:55 | ||||
chr19:52923448-52923559 | Common:2; Rare:48 | ||||
chr19:52942556-52942722 | Common:3; Rare:57 | ||||
chr19:53549427-53549678 | Common:1; Rare:32 | ||||
chr19:54207586-54207829 | Common:1; Rare:66 | ||||
chr19:56765267-56765372 | Rare:27 | ||||
chr19:57803955-57804298 | Common:3; Rare:89 | ||||
chr19:58550635-58550930 | Common:1; Rare:90 | ||||
chr2:2333207-2333352 | Rare:40 |