Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26257311-26257538 | Common:4; Rare:37 | ||||
chr1:26432091-26432404 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26787906-26787974 | Common:1; Rare:17; Clinvar (benign):1 | ||||
chr1:26890229-26890347 | Common:1; Rare:46 | ||||
chr1:27366890-27367164 | Common:1; Rare:56 | ||||
chr1:28505807-28506050 | Common:2; Rare:92 | ||||
chr1:28552882-28553116 | Common:2; Rare:87 | ||||
chr1:28643011-28643237 | Rare:88 | ||||
chr1:28668651-28668822 | Common:1; Rare:58 | ||||
chr1:28736733-28737018 | Common:1; Rare:99 | ||||
chr1:29181767-29181950 | Common:2; Rare:91 | ||||
chr1:31296743-31297054 | Common:4; Rare:100 | ||||
chr1:31372926-31373369 | Common:3; Rare:123 | ||||
chr1:32072792-32073004 | Rare:61 | ||||
chr1:32179581-32179768 | Rare:42 |