Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:70403752-70404283 | Common:3; Rare:713 | ||||
chr10:70404414-70404520 | Common:1; Rare:27 | ||||
chr10:70478140-70479100 | Common:4; Rare:410 | ||||
chr10:70602670-70603210 | Common:6; Rare:178; Clinvar:4 | ||||
chr10:70672180-70673680 | Common:51; Rare:1112 | ||||
chr10:70815641-70816041 | Common:1; Rare:239 | ||||
chr10:70816385-70816980 | Common:1; Rare:295 | ||||
chr10:70887644-70888136 | Common:7; Rare:217 | ||||
chr10:70888057-70888460 | Common:12; Rare:238 | ||||
chr10:70888483-70888883 | Common:7; Rare:226; Clinvar:17; Clinvar (benign):7 | ||||
chr10:71212230-71212769 | Common:8; Rare:504 | ||||
chr10:71318993-71319393 | Common:9; Rare:222; Clinvar:6; Clinvar (benign):3 | ||||
chr10:71319571-71319971 | Common:7; Rare:166 | ||||
chr10:71396565-71397071 | Common:8; Rare:165; Clinvar:3 | ||||
chr10:71712890-71713240 | Common:8; Rare:185 |