Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112956169-112956467 | Common:5; Rare:129; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073085-113073400 | Common:1; Rare:113 | ||||
chr1:113759883-113759970 | Rare:17 | ||||
chr1:113812222-113812593 | Common:2; Rare:149 | ||||
chr1:113905016-113905387 | Common:5; Rare:107 | ||||
chr1:114152920-114153052 | Common:2; Rare:36 | ||||
chr1:114581577-114581797 | Common:1; Rare:105 | ||||
chr1:114716671-114716843 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
chr1:114757916-114758103 | Common:3; Rare:60 | ||||
chr1:114780408-114780805 | Common:1; Rare:140 | ||||
chr1:115089420-115089612 | Common:2; Rare:76 | ||||
chr1:115841120-115841175 | Rare:7 | ||||
chr1:115976363-115976703 | Rare:126 | ||||
chr1:115976785-115976874 | Rare:23 | ||||
chr1:116372752-116372797 | Common:1; Rare:4 |