Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:201071609-201072041 | Rare:93 | ||||
chr2:201118601-201118857 | Rare:39 | ||||
chr2:201451548-201451826 | Common:2; Rare:75 | ||||
chr2:201642633-201642770 | Rare:68 | ||||
chr2:201780893-201781243 | Common:3; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
chr2:202238498-202238621 | Rare:40 | ||||
chr2:202912141-202912286 | Common:1; Rare:51 | ||||
chr2:203238779-203239042 | Common:1; Rare:93 | ||||
chr2:203328136-203328437 | Common:2; Rare:112 | ||||
chr2:206159380-206159989 | Common:4; Rare:182; Clinvar (benign):1 | ||||
chr2:206213332-206213591 | Common:1; Rare:37 | ||||
chr2:206274918-206275052 | Common:1; Rare:47 | ||||
chr2:206765305-206765662 | Common:3; Rare:91; Clinvar:4; Clinvar (benign):5 | ||||
chr2:207165947-207166099 | Rare:25 | ||||
chr2:207529774-207530046 | Common:3; Rare:80 |