Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:171434596-171434687 | Rare:29 | ||||
chr2:171894221-171894369 | Rare:63; Clinvar:1 | ||||
chr2:171922232-171922493 | Rare:99 | ||||
chr2:171999800-171999981 | Common:1; Rare:75 | ||||
chr2:174248460-174248725 | Common:1; Rare:80 | ||||
chr2:174395639-174395897 | Common:1; Rare:84 | ||||
chr2:174634553-174634621 | Rare:15 | ||||
chr2:175181629-175181804 | Common:4; Rare:73 | ||||
chr2:176002229-176002394 | Common:2; Rare:68 | ||||
chr2:176269378-176269499 | Common:1; Rare:49 | ||||
chr2:177212434-177212802 | Common:4; Rare:149 | ||||
chr2:177263528-177263741 | Common:2; Rare:56 | ||||
chr2:177392665-177392927 | Rare:91; Clinvar:5; Clinvar (benign):2 | ||||
chr2:177552764-177552838 | Common:1; Rare:25 | ||||
chr2:177618708-177619010 | Common:7; Rare:79 |