Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63593074-63593460 | Rare:115; Clinvar (benign):1 | ||||
chr1:64841302-64841509 | Rare:47; Clinvar:1 | ||||
chr1:64966409-64966699 | Common:2; Rare:105 | ||||
chr1:65309180-65309582 | Common:1; Rare:98 | ||||
chr1:66354312-66354651 | Common:1; Rare:45 | ||||
chr1:66533353-66533652 | Common:2; Rare:42 | ||||
chr1:66533895-66534199 | Common:1; Rare:73 | ||||
chr1:66924829-66925046 | Rare:87 | ||||
chr1:66925166-66925503 | Common:2; Rare:108 | ||||
chr1:66930067-66930394 | Rare:105 | ||||
chr1:67054384-67054451 | Common:1; Rare:21 | ||||
chr1:67307829-67307905 | Rare:27 | ||||
chr1:67429989-67430085 | Rare:35 | ||||
chr1:67430143-67430565 | Rare:154 | ||||
chr1:68232462-68232649 | Rare:43 |