Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:77219249-77219561 | Common:1; Rare:138 | ||||
chr1:77540618-77540808 | Common:3; Rare:43 | ||||
chr1:77540854-77541088 | Common:1; Rare:39 | ||||
chr1:77682096-77682259 | Rare:37 | ||||
chr1:77682349-77682756 | Common:1; Rare:91 | ||||
chr1:77682897-77683700 | Common:4; Rare:208 | ||||
chr1:77683844-77683930 | Rare:19 | ||||
chr1:77759114-77759310 | Rare:41 | ||||
chr1:77759544-77759607 | Rare:18 | ||||
chr1:77759665-77759953 | Common:2; Rare:116 | ||||
chr1:77779531-77779875 | Rare:107 | ||||
chr1:77780161-77780273 | Rare:16 | ||||
chr1:77888469-77888824 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77888827-77888926 | Common:1; Rare:23 | ||||
chr1:77888934-77889025 | Rare:25 |