Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:166839322-166839522 | Rare:57 | ||||
chr1:167935958-167936330 | Common:2; Rare:113 | ||||
chr1:167936553-167936953 | Common:1; Rare:141 | ||||
chr1:168178729-168179098 | Common:4; Rare:114 | ||||
chr1:168225720-168226066 | Common:4; Rare:109 | ||||
chr1:169367764-169368281 | Common:4; Rare:97 | ||||
chr1:169485705-169486219 | Common:2; Rare:150; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794868-169795079 | Common:3; Rare:50 | ||||
chr1:169893655-169893740 | Rare:29 | ||||
chr1:170074471-170074759 | Common:1; Rare:84 | ||||
chr1:170532028-170532210 | Rare:82; Clinvar:1 | ||||
chr1:170663029-170663162 | Rare:33 | ||||
chr1:170664035-170664344 | Common:4; Rare:83 | ||||
chr1:171485218-171485590 | Rare:108 | ||||
chr1:171741910-171742160 | Common:2; Rare:80 |