Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38899566-38899965 | Rare:111 | ||||
chr19:38930742-38930988 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391118-39391418 | Common:1; Rare:125 | ||||
chr19:39406706-39406848 | Rare:53 | ||||
chr19:39480602-39480888 | Common:3; Rare:141; Clinvar (pathogenic):1 | ||||
chr19:39846341-39846539 | Common:1; Rare:92 | ||||
chr19:39970957-39971196 | Common:3; Rare:62 | ||||
chr19:40056206-40056243 | Rare:5 | ||||
chr19:40090886-40090993 | Common:1; Rare:28 | ||||
chr19:40348393-40348739 | Common:4; Rare:112 | ||||
chr19:40751076-40751228 | Common:1; Rare:37 | ||||
chr19:40799085-40799210 | Common:3; Rare:47 | ||||
chr19:41219111-41219291 | Rare:37 | ||||
chr19:41397558-41397821 | Common:7; Rare:92; Clinvar (benign):4 | ||||
chr19:42132430-42132621 | Rare:36 |