Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:24360323-24360549 | Common:3; Rare:57 | ||||
chr2:24793028-24793161 | Rare:56 | ||||
chr2:24971907-24972153 | Common:1; Rare:79 | ||||
chr2:25878461-25878668 | Common:1; Rare:64 | ||||
chr2:25982427-25982885 | Common:1; Rare:113 | ||||
chr2:26033790-26034234 | Common:3; Rare:160 | ||||
chr2:26244581-26244943 | Common:2; Rare:132; Clinvar:5; Clinvar (benign):8 | ||||
chr2:26345764-26346160 | Common:2; Rare:121 | ||||
chr2:26401869-26401971 | Common:2; Rare:27 | ||||
chr2:26764210-26764305 | Rare:31 | ||||
chr2:27032872-27033004 | Rare:51 | ||||
chr2:27071599-27071839 | Common:1; Rare:72 | ||||
chr2:27134606-27134755 | Common:1; Rare:64 | ||||
chr2:27211931-27212109 | Common:3; Rare:67 | ||||
chr2:27212271-27212364 | Common:1; Rare:46 |