Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:166627950-166628073 | Rare:27 | ||||
chr6:166862326-166862394 | Common:1; Rare:26 | ||||
chr6:166862468-166862814 | Common:5; Rare:72 | ||||
chr6:166956523-166956724 | Common:4; Rare:72; Clinvar:3 | ||||
chr6:166999061-166999415 | Common:1; Rare:120 | ||||
chr6:167826397-167826578 | Common:5; Rare:52 | ||||
chr6:167826679-167827219 | Common:2; Rare:262 | ||||
chr6:167827537-167827664 | Common:1; Rare:51 | ||||
chr6:169253840-169254072 | Rare:35 | ||||
chr6:169701975-169702196 | Common:3; Rare:113 | ||||
chr6:169724420-169724843 | Rare:104 | ||||
chr6:169725468-169725746 | Common:3; Rare:80 | ||||
chr6:169751453-169751645 | Common:2; Rare:82; Clinvar (benign):1 | ||||
chr6:170290654-170290710 | Rare:8 | ||||
chr6:170290831-170290955 | Rare:35 |