Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:53786942-53787072 | Rare:49 | ||||
chr2:55050475-55050784 | Common:3; Rare:93 | ||||
chr2:61144921-61145147 | Common:2; Rare:77 | ||||
chr2:63841648-63841910 | Common:2; Rare:91 | ||||
chr2:65227591-65227857 | Rare:70 | ||||
chr2:68157548-68157931 | Common:1; Rare:194 | ||||
chr2:71130224-71130594 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
chr2:74147876-74148111 | Common:1; Rare:60; Clinvar:2 | ||||
chr2:74483001-74483095 | Rare:36 | ||||
chr2:74529680-74529966 | Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
chr2:86195395-86195623 | Common:5; Rare:79 | ||||
chr2:98608456-98608636 | Common:1; Rare:76 | ||||
chr2:101002177-101002304 | Rare:45 | ||||
chr2:105337273-105337573 | Common:5; Rare:105 | ||||
chr2:112584378-112584622 | Common:1; Rare:63 |