Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:63630050-63630133 | Common:1; Rare:15 | ||||
chr10:63630183-63630219 | Rare:8 | ||||
chr10:63707392-63707602 | Rare:37 | ||||
chr10:68340874-68341225 | Common:1; Rare:74 | ||||
chr10:68600355-68600481 | Rare:25 | ||||
chr10:68957102-68957233 | Common:2; Rare:23 | ||||
chr10:68959558-68959869 | Rare:50 | ||||
chr10:69061410-69061857 | Common:1; Rare:78 | ||||
chr10:70131179-70131323 | Rare:27 | ||||
chr10:71709185-71709263 | Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
chr10:71772155-71772457 | Common:3; Rare:52 | ||||
chr10:71817417-71817583 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
chr10:71825336-71825456 | Common:1; Rare:21 | ||||
chr10:71889103-71889213 | Common:3; Rare:21 | ||||
chr10:71965318-71965392 | Common:1; Rare:19 |