Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:25878431-25878742 | Common:3; Rare:88 | ||||
chr2:26033775-26034159 | Common:4; Rare:140 | ||||
chr2:26034529-26034644 | Rare:42 | ||||
chr2:26194568-26194767 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr2:26244581-26244990 | Common:2; Rare:150; Clinvar:5; Clinvar (benign):9 | ||||
chr2:26345798-26346165 | Common:1; Rare:110 | ||||
chr2:27032867-27033009 | Rare:53 | ||||
chr2:27071560-27071864 | Common:1; Rare:91 | ||||
chr2:27134615-27134834 | Common:1; Rare:83 | ||||
chr2:27211794-27212103 | Common:3; Rare:104 | ||||
chr2:27212252-27212370 | Common:1; Rare:59 | ||||
chr2:27323043-27323141 | Rare:25; Clinvar (benign):1 | ||||
chr2:27356754-27356863 | Rare:29 | ||||
chr2:27356961-27357199 | Common:2; Rare:87 | ||||
chr2:27370310-27370641 | Common:1; Rare:131 |