Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111140041-111140305 | Common:2; Rare:90 | ||||
chr1:111473760-111474003 | Common:2; Rare:50 | ||||
chr1:111619727-111619981 | Common:2; Rare:83 | ||||
chr1:111739367-111739579 | Common:3; Rare:57 | ||||
chr1:112396061-112396265 | Common:1; Rare:65 | ||||
chr1:112619099-112619236 | Rare:49 | ||||
chr1:112619643-112619871 | Common:1; Rare:82 | ||||
chr1:112707080-112707230 | Rare:52 | ||||
chr1:112956129-112956473 | Common:5; Rare:142; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073100-113073255 | Common:1; Rare:67 | ||||
chr1:113390236-113390495 | Common:1; Rare:66 | ||||
chr1:113812232-113812587 | Common:2; Rare:144 | ||||
chr1:113904824-113905445 | Common:7; Rare:182; Clinvar (benign):1 | ||||
chr1:115089391-115089644 | Common:3; Rare:97 | ||||
chr1:116570967-116571135 | Common:1; Rare:52 |