Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42456010-42456608 | Common:2; Rare:185 | ||||
chr1:42658324-42658463 | Rare:44 | ||||
chr1:42682157-42682463 | Common:2; Rare:81 | ||||
chr1:42683325-42683466 | Common:2; Rare:53 | ||||
chr1:42767003-42767303 | Common:4; Rare:96; Clinvar (benign):1 | ||||
chr1:42816932-42817139 | Common:1; Rare:59 | ||||
chr1:42817198-42817538 | Rare:114 | ||||
chr1:42846401-42846638 | Common:1; Rare:65 | ||||
chr1:42958858-42959042 | Common:1; Rare:49; Clinvar:4; Clinvar (benign):2 | ||||
chr1:43172170-43172452 | Common:3; Rare:122 | ||||
chr1:43358662-43358986 | Common:7; Rare:102 | ||||
chr1:43366300-43366602 | Common:3; Rare:61 | ||||
chr1:43367916-43368180 | Rare:66 | ||||
chr1:43389757-43389955 | Common:3; Rare:90 | ||||
chr1:43946569-43946983 | Rare:109 |