Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:209793368-209793465 | Rare:14 | ||||
chr1:209795214-209795437 | Common:2; Rare:63; Clinvar (benign):2 | ||||
chr1:209797405-209797747 | Common:2; Rare:47 | ||||
chr1:209797787-209798083 | Common:1; Rare:33 | ||||
chr1:209798093-209798171 | Common:4; Rare:7 | ||||
chr1:209798248-209798348 | Common:3; Rare:13 | ||||
chr1:209798992-209799318 | Rare:49 | ||||
chr1:209800542-209800779 | Common:2; Rare:38 | ||||
chr1:209801448-209801531 | Common:1; Rare:19 | ||||
chr1:209803974-209804344 | Rare:65 | ||||
chr1:209804631-209804925 | Common:2; Rare:47 | ||||
chr1:209805349-209805434 | Common:1; Rare:11 | ||||
chr1:209806859-209806886 | Rare:4 | ||||
chr1:209807678-209807903 | Common:3; Rare:40 | ||||
chr1:209816059-209816219 | Common:2; Rare:32 |