Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:159712372-159712584 | Common:2; Rare:85 | ||||
chr2:161308301-161308533 | Common:2; Rare:67 | ||||
chr2:162243348-162243624 | Common:1; Rare:52 | ||||
chr2:162344085-162344156 | Rare:28 | ||||
chr2:169510118-169510386 | Rare:77; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr2:169584764-169584809 | Rare:14 | ||||
chr2:170928913-170929327 | Common:5; Rare:121 | ||||
chr2:171433976-171434248 | Common:2; Rare:69 | ||||
chr2:171522282-171522525 | Common:3; Rare:57 | ||||
chr2:171922332-171922499 | Rare:68 | ||||
chr2:171999806-171999985 | Common:1; Rare:74 | ||||
chr2:173354602-173354893 | Common:1; Rare:86 | ||||
chr2:173963819-173963927 | Common:1; Rare:53 | ||||
chr2:174248456-174248758 | Common:1; Rare:94 | ||||
chr2:174395629-174395800 | Common:1; Rare:57 |