Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160262094-160262240 | Rare:39 | ||||
chr1:160262382-160262715 | Common:1; Rare:98 | ||||
chr1:160343148-160343400 | Rare:97 | ||||
chr1:160400421-160400626 | Common:2; Rare:51 | ||||
chr1:160647019-160647098 | Rare:14 | ||||
chr1:160711781-160711882 | Common:2; Rare:23 | ||||
chr1:161020762-161020945 | Rare:46 | ||||
chr1:161021016-161021507 | Common:6; Rare:135 | ||||
chr1:161045879-161046057 | Common:1; Rare:46 | ||||
chr1:161089418-161089742 | Rare:75 | ||||
chr1:161117953-161118155 | Rare:102 | ||||
chr1:161132417-161132709 | Common:1; Rare:95 | ||||
chr1:161159410-161159526 | Common:1; Rare:31 | ||||
chr1:161166220-161166511 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161199053-161199298 | Rare:39 |