Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35648110-35648402 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr19:35745369-35745698 | Rare:97 | ||||
chr19:35748253-35748583 | Common:1; Rare:94 | ||||
chr19:35757874-35758205 | Common:2; Rare:99 | ||||
chr19:35899713-35899863 | Common:1; Rare:46 | ||||
chr19:35900538-35900623 | Rare:16 | ||||
chr19:36014192-36014517 | Common:2; Rare:91 | ||||
chr19:36054359-36054589 | Common:3; Rare:63 | ||||
chr19:36114808-36114991 | Common:2; Rare:79 | ||||
chr19:36115672-36115755 | Rare:26 | ||||
chr19:36139860-36140093 | Rare:69 | ||||
chr19:36214637-36214748 | Common:1; Rare:33 | ||||
chr19:36215070-36215193 | Rare:38 | ||||
chr19:36489510-36489644 | Common:1; Rare:31 | ||||
chr19:36528230-36528444 | Common:1; Rare:51 |