Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39672052-39672233 | Common:2; Rare:56 | ||||
chr1:39883428-39883570 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:40040437-40040799 | Common:3; Rare:109 | ||||
chr1:40161264-40161399 | Rare:36 | ||||
chr1:40257903-40258292 | Common:4; Rare:108; Clinvar:7; Clinvar (benign):1 | ||||
chr1:40374527-40374645 | Common:12; Rare:27 | ||||
chr1:40450025-40450145 | Common:1; Rare:43 | ||||
chr1:40508626-40508810 | Common:6; Rare:57 | ||||
chr1:40531502-40531857 | Common:2; Rare:77 | ||||
chr1:40691495-40691865 | Common:3; Rare:166 | ||||
chr1:40692033-40692111 | Rare:31 | ||||
chr1:40709148-40709461 | Rare:75 | ||||
chr1:40979636-40979766 | Common:1; Rare:45 | ||||
chr1:41242091-41242403 | Rare:92 | ||||
chr1:42335114-42335408 | Common:6; Rare:146 |