Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:97920840-97921320 | Common:2; Rare:246; Clinvar:6; Clinvar (pathogenic):1 | ||||
chr1:99645501-99646420 | Common:2; Rare:483 | ||||
chr1:99646343-99647624 | Common:6; Rare:316 | ||||
chr1:99765007-99765701 | Common:2; Rare:161 | ||||
chr1:99765617-99766105 | Rare:204 | ||||
chr1:99766083-99766483 | Common:1; Rare:59 | ||||
chr1:99766440-99767101 | Common:6; Rare:284 | ||||
chr1:99849391-99849791 | Common:6; Rare:113 | ||||
chr1:99849800-99850750 | Common:6; Rare:710; Clinvar:6; Clinvar (benign):6 | ||||
chr1:99969271-99969671 | Common:1; Rare:71 | ||||
chr1:99969864-99970139 | Common:2; Rare:335 | ||||
chr1:99970150-99970260 | Common:1; Rare:23 | ||||
chr1:99970299-99970699 | Common:3; Rare:278 | ||||
chr1:99992738-99993860 | Common:13; Rare:236; Clinvar:3; Clinvar (benign):6 | ||||
chr1:100037890-100038239 | Common:6; Rare:525 |