Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35337632-35337713 | Rare:9 | ||||
chr19:35345845-35346120 | Common:5; Rare:54 | ||||
chr19:35346136-35346546 | Common:7; Rare:93 | ||||
chr19:35609884-35610282 | Rare:70 | ||||
chr19:35625340-35625616 | Rare:46 | ||||
chr19:35889074-35889215 | Rare:30 | ||||
chr19:36125453-36125737 | Rare:96 | ||||
chr19:38034216-38034530 | Common:1; Rare:50 | ||||
chr19:38083230-38083396 | Rare:33 | ||||
chr19:38608070-38608167 | Common:2; Rare:27 | ||||
chr19:39392170-39392470 | Rare:61 | ||||
chr19:39403723-39404182 | Common:1; Rare:94 | ||||
chr19:39953431-39953749 | Common:1; Rare:43 | ||||
chr19:41297667-41297882 | Common:1; Rare:32 | ||||
chr19:41331948-41332161 | Rare:48; Clinvar (benign):1 |