Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101806079-101806207 | Common:1; Rare:27 | ||||
chr10:101812160-101812186 | Rare:4 | ||||
chr10:101812653-101813072 | Rare:115 | ||||
chr10:102121339-102121532 | Rare:23 | ||||
chr10:102134012-102134140 | Rare:29 | ||||
chr10:102138940-102139301 | Common:1; Rare:100 | ||||
chr10:102152981-102153165 | Common:1; Rare:27 | ||||
chr10:102396674-102396997 | Rare:66; Clinvar (benign):1 | ||||
chr10:102397021-102397407 | Common:1; Rare:90; Clinvar (benign):1 | ||||
chr10:102643269-102643426 | Common:3; Rare:34 | ||||
chr10:102919627-102919792 | Rare:28 | ||||
chr10:103101287-103101470 | Common:1; Rare:43; Clinvar:1; Clinvar (benign):1 | ||||
chr10:103176336-103176583 | Common:1; Rare:46 | ||||
chr10:103192557-103192679 | Rare:27 | ||||
chr10:103615771-103616045 | Common:1; Rare:35 |