Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111755507-111755744 | Common:3; Rare:81 | ||||
chr1:112396003-112396265 | Common:1; Rare:82 | ||||
chr1:112619109-112619242 | Rare:47 | ||||
chr1:112619637-112619880 | Common:2; Rare:87 | ||||
chr1:112699704-112699939 | Common:1; Rare:69 | ||||
chr1:112707068-112707220 | Rare:50 | ||||
chr1:112956169-112956504 | Common:5; Rare:140; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073068-113073255 | Common:1; Rare:78 | ||||
chr1:113390391-113390536 | Common:1; Rare:43 | ||||
chr1:113759471-113759598 | Common:1; Rare:41 | ||||
chr1:113811999-113812090 | Common:1; Rare:32 | ||||
chr1:113812436-113812608 | Rare:54 | ||||
chr1:113904793-113905467 | Common:7; Rare:190; Clinvar (benign):1 | ||||
chr1:113929510-113929814 | Common:2; Rare:77 | ||||
chr1:114581577-114581818 | Common:1; Rare:111 |