Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:69914767-69915181 | Common:1; Rare:101 | ||||
chr2:69961422-69961994 | Common:1; Rare:186; Clinvar:1 | ||||
chr2:70086931-70087114 | Common:1; Rare:92 | ||||
chr2:70087850-70088548 | Common:1; Rare:184 | ||||
chr2:70258007-70258203 | Common:2; Rare:73 | ||||
chr2:71068526-71068662 | Rare:67 | ||||
chr2:71129771-71129932 | Rare:32 | ||||
chr2:71130178-71130662 | Common:6; Rare:139; Clinvar:1; Clinvar (benign):2 | ||||
chr2:73233200-73233440 | Common:1; Rare:63 | ||||
chr2:73234182-73234368 | Common:2; Rare:57 | ||||
chr2:74147875-74148042 | Common:1; Rare:42; Clinvar:2 | ||||
chr2:74441840-74442066 | Common:2; Rare:53 | ||||
chr2:74465367-74465436 | Rare:16 | ||||
chr2:74482967-74483129 | Common:1; Rare:69 | ||||
chr2:74507664-74507790 | Rare:27 |