Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946237-53946428 | Rare:72 | ||||
chr1:53946545-53946654 | Common:1; Rare:27 | ||||
chr1:54018170-54018309 | Rare:44 | ||||
chr1:54053178-54053688 | Common:6; Rare:167 | ||||
chr1:54153830-54154080 | Rare:46 | ||||
chr1:54199933-54200250 | Rare:85 | ||||
chr1:54406383-54406574 | Common:3; Rare:81 | ||||
chr1:54542068-54542242 | Common:2; Rare:56 | ||||
chr1:54542539-54542760 | Common:1; Rare:44 | ||||
chr1:54715723-54715920 | Common:3; Rare:65 | ||||
chr1:54764420-54764836 | Common:7; Rare:126; Clinvar (benign):1 | ||||
chr1:54801306-54801672 | Common:3; Rare:67 | ||||
chr1:54887152-54887455 | Common:3; Rare:96; Clinvar:2; Clinvar (benign):1 | ||||
chr1:55039357-55039633 | Common:2; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
chr1:55214632-55214737 | Common:1; Rare:31 |