Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6451169-6451356 | Rare:26 | ||||
chr1:6602865-6603111 | Common:3; Rare:88 | ||||
chr1:7961482-7961792 | Common:3; Rare:99; Clinvar:3; Clinvar (benign):3 | ||||
chr1:8026310-8026500 | Common:2; Rare:80 | ||||
chr1:8878578-8878835 | Rare:130 | ||||
chr1:9239778-9239914 | Common:2; Rare:26 | ||||
chr1:9943051-9943497 | Common:6; Rare:113 | ||||
chr1:10398860-10399125 | Common:2; Rare:103 | ||||
chr1:10399365-10399498 | Common:2; Rare:29 | ||||
chr1:11055809-11056090 | Rare:78 | ||||
chr1:11262490-11262817 | Common:2; Rare:101 | ||||
chr1:11273269-11273515 | Common:2; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
chr1:11654351-11654541 | Rare:50 | ||||
chr1:11654817-11654925 | Common:2; Rare:32 | ||||
chr1:11805896-11806252 | Common:2; Rare:98; Clinvar:1 |