Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:203014626-203014952 | Common:1; Rare:105 | ||||
chr2:203238893-203239057 | Common:2; Rare:68 | ||||
chr2:203239272-203239351 | Rare:30 | ||||
chr2:203328047-203328616 | Common:2; Rare:184 | ||||
chr2:203328847-203328954 | Rare:36 | ||||
chr2:203535127-203535284 | Rare:34 | ||||
chr2:203535419-203535502 | Rare:31 | ||||
chr2:205682353-205682651 | Rare:59 | ||||
chr2:206085807-206085986 | Common:1; Rare:51 | ||||
chr2:206086204-206086452 | Rare:43 | ||||
chr2:206159178-206159927 | Common:6; Rare:196; Clinvar (benign):2 | ||||
chr2:206443318-206443622 | Common:1; Rare:112 | ||||
chr2:206765278-206765668 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165766-207166346 | Common:2; Rare:152 | ||||
chr2:207166801-207166988 | Common:2; Rare:78 |