Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16613400-16613605 | Common:2 | ||||
chr1:17053960-17054374 | Common:3; Rare:128; Clinvar:16; Clinvar (benign):10 | ||||
chr1:17119449-17119599 | Rare:43 | ||||
chr1:17439310-17439379 | Common:1; Rare:14 | ||||
chr1:17439669-17439926 | Rare:86 | ||||
chr1:19210071-19210533 | Common:1; Rare:150 | ||||
chr1:19210705-19210939 | Rare:41 | ||||
chr1:19251473-19252018 | Common:9; Rare:178 | ||||
chr1:19311972-19312358 | Common:8; Rare:174 | ||||
chr1:19484259-19484425 | Common:1; Rare:74 | ||||
chr1:19485440-19485762 | Common:1; Rare:120 | ||||
chr1:19596835-19597068 | Common:2; Rare:101 | ||||
chr1:19643513-19643752 | Common:2; Rare:40 | ||||
chr1:19799878-19800228 | Common:4; Rare:97 | ||||
chr1:19882577-19882888 | Rare:73 |