Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99659271-99659515 | Common:1; Rare:60 | ||||
chr10:99732088-99732319 | Rare:80; Clinvar:3 | ||||
chr10:100185938-100186110 | Rare:69 | ||||
chr10:100267624-100267746 | Common:2; Rare:34 | ||||
chr10:100346877-100347276 | Common:1; Rare:97 | ||||
chr10:100912776-100912974 | Common:1; Rare:52 | ||||
chr10:100987437-100987598 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
chr10:100996965-100997109 | Common:1; Rare:46 | ||||
chr10:101588211-101588339 | Rare:51 | ||||
chr10:101818393-101818762 | Common:1; Rare:99 | ||||
chr10:102114962-102115255 | Common:2; Rare:82 | ||||
chr10:102152090-102152420 | Common:3; Rare:108 | ||||
chr10:102714271-102714627 | Common:2; Rare:119 | ||||
chr10:102854167-102854285 | Common:1; Rare:41 | ||||
chr10:103396411-103396693 | Rare:100 |