Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49491464-49491985 | Common:3; Rare:152 | ||||
chr19:49496966-49497268 | Common:2; Rare:93 | ||||
chr19:49640731-49640863 | Rare:17 | ||||
chr19:50190503-50190768 | Common:2; Rare:55 | ||||
chr19:50205242-50205486 | Common:1; Rare:63 | ||||
chr19:50419653-50419832 | Common:1; Rare:45 | ||||
chr19:52786086-52786149 | Rare:8 | ||||
chr19:52923398-52923550 | Common:3; Rare:64 | ||||
chr19:52942539-52942766 | Common:8; Rare:84 | ||||
chr19:53549427-53549491 | Rare:8 | ||||
chr19:54124442-54124558 | Common:1; Rare:47; Clinvar (benign):1 | ||||
chr19:54128792-54129123 | Common:5; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
chr19:54158430-54158733 | Common:2; Rare:68 | ||||
chr19:54162231-54162490 | Common:11; Rare:86 | ||||
chr19:54455123-54455445 | Common:4; Rare:86 |