Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:178871000-178871151 | Rare:26 | ||||
chr1:179877747-179877896 | Rare:34 | ||||
chr1:179881997-179882341 | Common:4; Rare:81 | ||||
chr1:179882502-179882924 | Rare:212; Clinvar:9; Clinvar (benign):2 | ||||
chr1:181088494-181088707 | Rare:70 | ||||
chr1:182391316-182391478 | Rare:32 | ||||
chr1:182604381-182604541 | Rare:37 | ||||
chr1:182789583-182789796 | Common:2; Rare:70 | ||||
chr1:183635635-183636094 | Common:4; Rare:130 | ||||
chr1:185156941-185157303 | Common:1; Rare:100 | ||||
chr1:185317193-185317468 | Common:1; Rare:82 | ||||
chr1:186375099-186375484 | Rare:113 | ||||
chr1:186375557-186375967 | Common:1; Rare:116 | ||||
chr1:186680319-186680697 | Common:3; Rare:80 | ||||
chr1:193059314-193059440 | Rare:48 |