Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:30026569-30026994 | Common:1; Rare:99 | ||||
chr7:30478681-30478857 | Common:1; Rare:69; Clinvar:1 | ||||
chr7:30504780-30505049 | Common:1; Rare:84 | ||||
chr7:30594727-30595095 | Common:6; Rare:174; Clinvar:9; Clinvar (benign):13 | ||||
chr7:32495268-32495564 | Rare:75 | ||||
chr7:33062702-33062895 | Common:2; Rare:85 | ||||
chr7:35800723-35801269 | Common:2; Rare:208 | ||||
chr7:39566267-39566458 | Common:1; Rare:91 | ||||
chr7:39623475-39623812 | Rare:107 | ||||
chr7:40134558-40135053 | Rare:155; Clinvar:1 | ||||
chr7:41703069-41703270 | Common:1; Rare:28 | ||||
chr7:42932144-42932410 | Rare:107 | ||||
chr7:43869458-43869671 | Rare:66 | ||||
chr7:43926368-43926463 | Rare:32 | ||||
chr7:44044617-44044740 | Common:1; Rare:32 |