Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:70976947-70977135 | Common:4; Rare:38 | ||||
chr2:71945312-71945608 | Common:1; Rare:59 | ||||
chr2:72144950-72145280 | Common:1; Rare:86 | ||||
chr2:72148920-72149160 | Rare:60 | ||||
chr2:73981386-73981469 | Rare:21 | ||||
chr2:73983837-73984132 | Rare:52 | ||||
chr2:74120116-74120377 | Common:1; Rare:88 | ||||
chr2:74377442-74377691 | Common:1; Rare:64 | ||||
chr2:74703436-74703721 | Common:5; Rare:51 | ||||
chr2:74714994-74715310 | Rare:65 | ||||
chr2:85343232-85343536 | Rare:75 | ||||
chr2:85537678-85537971 | Common:3; Rare:75 | ||||
chr2:85540352-85540507 | Rare:32 | ||||
chr2:85542632-85543043 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):9 | ||||
chr2:85886695-85886860 | Common:1; Rare:31 |