Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45011303-45011432 | Rare:31 | ||||
chr1:45012004-45012278 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
chr1:45206550-45206695 | Rare:48 | ||||
chr1:45326650-45326980 | Rare:72 | ||||
chr1:45339619-45339737 | Rare:23 | ||||
chr1:45339955-45340247 | Rare:107; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr1:45340282-45340598 | Common:2; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr1:45491132-45491419 | Common:2; Rare:73 | ||||
chr1:45499932-45500386 | Common:2; Rare:116; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr1:45521814-45522090 | Common:1; Rare:102 | ||||
chr1:45550667-45551086 | Common:4; Rare:109 | ||||
chr1:45583300-45583640 | Common:3; Rare:86 | ||||
chr1:45583809-45584068 | Common:1; Rare:85 | ||||
chr1:45686151-45686286 | Rare:39 | ||||
chr1:45686475-45686705 | Rare:89 |