Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:18108870-18109150 | Common:4; Rare:71 | ||||
chr19:18136070-18136320 | Common:2; Rare:68 | ||||
chr19:18279470-18279920 | Rare:247 | ||||
chr19:18303380-18303710 | Rare:92 | ||||
chr19:18304300-18304780 | Common:5; Rare:176 | ||||
chr19:18318151-18318897 | Common:1; Rare:287 | ||||
chr19:18319830-18320050 | Rare:49 | ||||
chr19:18372704-18373161 | Common:5; Rare:174 | ||||
chr19:18373830-18374090 | Rare:78 | ||||
chr19:18380080-18380630 | Common:5; Rare:154 | ||||
chr19:18514750-18515250 | Rare:173 | ||||
chr19:18599551-18600151 | Common:4; Rare:283; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr19:19097000-19097380 | Common:4; Rare:159 | ||||
chr19:19098750-19099070 | Rare:105 | ||||
chr19:19667864-19668264 | Common:4; Rare:103 |