Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:164955484-164955653 | Rare:40 | ||||
chr2:165794122-165794315 | Common:2; Rare:53; Clinvar:6; Clinvar (benign):1 | ||||
chr2:169584317-169584622 | Common:1; Rare:118 | ||||
chr2:169584744-169584809 | Rare:15 | ||||
chr2:169694334-169694590 | Common:5; Rare:90 | ||||
chr2:169798767-169798965 | Rare:51 | ||||
chr2:171433941-171434234 | Common:3; Rare:76 | ||||
chr2:171894212-171894358 | Rare:63; Clinvar:1 | ||||
chr2:171922288-171922503 | Rare:82 | ||||
chr2:171999831-171999972 | Common:1; Rare:58 | ||||
chr2:173354566-173354918 | Common:1; Rare:107 | ||||
chr2:173965295-173965515 | Common:1; Rare:79 | ||||
chr2:174248465-174248747 | Common:1; Rare:84 | ||||
chr2:174395639-174395805 | Common:1; Rare:55 | ||||
chr2:174486977-174487385 | Common:2; Rare:99 |