Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:158818220-158818355 | Common:3; Rare:52 | ||||
chr6:158819316-158819450 | Common:2; Rare:50 | ||||
chr6:159000141-159000322 | Common:1; Rare:44 | ||||
chr6:159693176-159693454 | Common:5; Rare:92 | ||||
chr6:159726918-159727175 | Common:1; Rare:100 | ||||
chr6:159789538-159790008 | Common:5; Rare:156 | ||||
chr6:162727724-162727977 | Rare:81; Clinvar:1 | ||||
chr6:166342478-166342657 | Common:5; Rare:76 | ||||
chr6:166999017-166999424 | Common:1; Rare:137 | ||||
chr6:167826820-167827191 | Common:2; Rare:182 | ||||
chr6:169701993-169702161 | Common:1; Rare:75 | ||||
chr6:169751563-169751661 | Rare:41; Clinvar (benign):2 | ||||
chr6:170306548-170306824 | Common:3; Rare:90 | ||||
chr6:170554219-170554426 | Common:1; Rare:66 | ||||
chr7:519153-519324 | Rare:42 |