Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19800139-19800280 | Common:2; Rare:29 | ||||
chr1:19882162-19882536 | Common:6; Rare:176 | ||||
chr1:19882760-19883758 | Common:7; Rare:258 | ||||
chr1:20484127-20484409 | Common:1; Rare:65 | ||||
chr1:20484663-20484801 | Common:2; Rare:29 | ||||
chr1:20485310-20486058 | Common:2; Rare:239 | ||||
chr1:20486131-20486257 | Rare:30 | ||||
chr1:20486179-20486407 | Rare:93 | ||||
chr1:20486703-20486846 | Common:1; Rare:40 | ||||
chr1:20508027-20508288 | Common:9; Rare:216 | ||||
chr1:20633361-20633555 | Rare:82 | ||||
chr1:20633770-20634220 | Common:3; Rare:202; Clinvar (benign):2 | ||||
chr1:20660846-20661246 | Common:5; Rare:160; Clinvar:2; Clinvar (benign):4 | ||||
chr1:20661318-20661924 | Common:10; Rare:464; Clinvar:12; Clinvar (benign):18 | ||||
chr1:20717770-20718602 | Common:4; Rare:388 |