Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:12068878-12069014 | Rare:60 | ||||
chr10:12129451-12129719 | Rare:109 | ||||
chr10:12195819-12195974 | Rare:38 | ||||
chr10:13099717-13099935 | Common:1; Rare:52 | ||||
chr10:13099990-13100279 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):6 | ||||
chr10:13116147-13116335 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr10:13348006-13348352 | Rare:113 | ||||
chr10:14532672-14532917 | Common:2; Rare:57 | ||||
chr10:14604247-14604515 | Common:4; Rare:117 | ||||
chr10:14838029-14838391 | Common:2; Rare:103 | ||||
chr10:14878637-14878884 | Common:2; Rare:73 | ||||
chr10:14954023-14954321 | Common:1; Rare:95 | ||||
chr10:15097301-15097409 | Common:1; Rare:52 | ||||
chr10:16817322-16817734 | Common:5; Rare:145 | ||||
chr10:17228110-17228241 | Common:1; Rare:26 |