Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42455998-42456103 | Rare:35 | ||||
chr1:42456233-42456592 | Common:1; Rare:113 | ||||
chr1:42658295-42658449 | Common:2; Rare:45 | ||||
chr1:42682158-42682442 | Common:2; Rare:71 | ||||
chr1:42682608-42682731 | Common:1; Rare:50 | ||||
chr1:42767023-42767309 | Common:4; Rare:88 | ||||
chr1:42816992-42817136 | Common:1; Rare:37 | ||||
chr1:42817225-42817577 | Rare:118 | ||||
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958858-42959042 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43367931-43368169 | Rare:58 | ||||
chr1:43389765-43389956 | Common:4; Rare:83 | ||||
chr1:43946504-43946865 | Rare:98 | ||||
chr1:43974763-43975042 | Common:3; Rare:77 | ||||
chr1:44775487-44775599 | Rare:48 |