Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154183002-154183465 | Rare:136 | ||||
chr1:154220507-154221016 | Common:1; Rare:172 | ||||
chr1:154221252-154221372 | Rare:30 | ||||
chr1:154257146-154257414 | Rare:67 | ||||
chr1:154272292-154272791 | Common:6; Rare:125; Clinvar:3; Clinvar (benign):4 | ||||
chr1:154320967-154321127 | Rare:31 | ||||
chr1:154627864-154628015 | Common:3; Rare:76 | ||||
chr1:154936672-154936762 | Common:2; Rare:29 | ||||
chr1:154956085-154956235 | Common:1; Rare:42 | ||||
chr1:154961676-154962059 | Common:1; Rare:128 | ||||
chr1:154970726-154970852 | Rare:23 | ||||
chr1:154974338-154974730 | Rare:101 | ||||
chr1:154983091-154983393 | Common:2; Rare:59; Clinvar (benign):1 | ||||
chr1:155051150-155051368 | Common:2; Rare:72 | ||||
chr1:155085392-155085536 | Common:1; Rare:34 |