Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:100529831-100529987 | Common:1; Rare:44 | ||||
chr10:100912751-100913038 | Common:1; Rare:89 | ||||
chr10:100987274-100987621 | Common:2; Rare:125; Clinvar:1; Clinvar (benign):2 | ||||
chr10:101031113-101031302 | Common:1; Rare:40 | ||||
chr10:101588166-101588336 | Rare:71 | ||||
chr10:101817982-101818053 | Rare:23 | ||||
chr10:101818315-101818762 | Common:1; Rare:125 | ||||
chr10:102152083-102152432 | Common:3; Rare:117 | ||||
chr10:102394359-102394563 | Rare:59 | ||||
chr10:102395566-102395735 | Common:1; Rare:47 | ||||
chr10:102714271-102714655 | Common:2; Rare:127 | ||||
chr10:102776041-102776228 | Common:1; Rare:27 | ||||
chr10:102854133-102854285 | Common:1; Rare:56 | ||||
chr10:103193243-103193527 | Common:5; Rare:82; Clinvar (benign):1 | ||||
chr10:103396386-103396709 | Rare:118 |