Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15526553-15526917 | Common:2; Rare:117 | ||||
chr1:15758749-15758817 | Common:1; Rare:17 | ||||
chr1:16017929-16018251 | Common:7; Rare:111 | ||||
chr1:16352401-16352564 | Common:2; Rare:90 | ||||
chr1:16613486-16613648 | Common:1 | ||||
chr1:17053991-17054316 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):8 | ||||
chr1:17439706-17439871 | Rare:55 | ||||
chr1:19210071-19210533 | Common:1; Rare:150 | ||||
chr1:19251494-19251854 | Common:6; Rare:121 | ||||
chr1:19312033-19312350 | Common:8; Rare:154 | ||||
chr1:19484396-19484565 | Rare:48 | ||||
chr1:19485435-19485775 | Common:1; Rare:127 | ||||
chr1:19799924-19800245 | Common:4; Rare:82 | ||||
chr1:20185988-20186138 | Common:1; Rare:52 | ||||
chr1:20486188-20486384 | Rare:48 |