Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:92830974-92831172 | Rare:32 | ||||
chr10:95434723-95434949 | Common:1; Rare:39 | ||||
chr10:95877194-95877403 | Rare:34 | ||||
chr10:96272801-96272935 | Rare:40 | ||||
chr10:96595609-96595880 | Rare:59; Clinvar (benign):1 | ||||
chr10:96673927-96674079 | Rare:22 | ||||
chr10:96935919-96936050 | Rare:26 | ||||
chr10:97333705-97333859 | Rare:37 | ||||
chr10:97406243-97406360 | Rare:19 | ||||
chr10:97430805-97431164 | Rare:111 | ||||
chr10:98435482-98435733 | Common:2; Rare:54; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr10:99431378-99431506 | Rare:26 | ||||
chr10:99526469-99526556 | Common:1; Rare:16 | ||||
chr10:99613347-99613389 | Rare:4 | ||||
chr10:99727058-99727345 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 |