Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39403704-39404010 | Rare:53 | ||||
chr19:39539235-39539453 | Common:1; Rare:52 | ||||
chr19:41331873-41332231 | Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
chr19:41352845-41352926 | Rare:16 | ||||
chr19:41531541-41531736 | Common:1; Rare:45 | ||||
chr19:41888027-41888117 | Common:1; Rare:20 | ||||
chr19:42292831-42292993 | Rare:58; Clinvar:2 | ||||
chr19:42396902-42397194 | Common:1; Rare:68 | ||||
chr19:44752181-44752346 | Rare:27 | ||||
chr19:45456161-45456328 | Rare:41 | ||||
chr19:48913193-48913510 | Common:4; Rare:97 | ||||
chr19:49492265-49492361 | Common:1; Rare:27 | ||||
chr19:52941444-52941757 | Common:2; Rare:87 | ||||
chr19:52942536-52942767 | Common:8; Rare:85 | ||||
chr19:53102377-53102562 | Rare:44 |