Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:38686688-38687109 | Common:5; Rare:111; Clinvar:3; Clinvar (benign):1 | ||||
chr13:39038012-39038429 | Common:1; Rare:110 | ||||
chr13:39038583-39038630 | Rare:21 | ||||
chr13:39603114-39603284 | Common:1; Rare:56 | ||||
chr13:39655618-39655735 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr13:40771071-40771245 | Common:1; Rare:74 | ||||
chr13:41060897-41061011 | Common:16; Rare:73 | ||||
chr13:41061194-41061633 | Common:3; Rare:153 | ||||
chr13:41132719-41132980 | Rare:70 | ||||
chr13:41194459-41194652 | Common:2; Rare:48 | ||||
chr13:41457355-41457547 | Common:2; Rare:58 | ||||
chr13:43786814-43786847 | Common:1; Rare:10 | ||||
chr13:43786912-43786967 | Rare:19 | ||||
chr13:43879464-43879615 | Rare:42 | ||||
chr13:43879718-43879885 | Common:18; Rare:53 |