Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:158819323-158819424 | Common:2; Rare:42 | ||||
chr6:158999807-158999886 | Rare:30 | ||||
chr6:159693171-159693587 | Common:6; Rare:120 | ||||
chr6:159726918-159727185 | Common:1; Rare:101 | ||||
chr6:159727315-159727616 | Common:5; Rare:127 | ||||
chr6:159789553-159789958 | Common:4; Rare:135 | ||||
chr6:159790257-159790506 | Common:7; Rare:80 | ||||
chr6:160991676-160991785 | Common:1; Rare:41 | ||||
chr6:162727124-162727156 | Common:1; Rare:7 | ||||
chr6:162727724-162728070 | Common:3; Rare:106; Clinvar:1 | ||||
chr6:166342519-166342653 | Common:3; Rare:51 | ||||
chr6:166999074-166999410 | Common:1; Rare:114 | ||||
chr6:169701973-169702184 | Common:3; Rare:105 | ||||
chr6:169751507-169751644 | Rare:49; Clinvar (benign):1 | ||||
chr6:170306548-170306808 | Common:1; Rare:87 |