Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:37989914-37990190 | Rare:90 | ||||
chr1:38012421-38012823 | Common:1; Rare:118 | ||||
chr1:38859707-38859984 | Rare:108 | ||||
chr1:38873281-38873556 | Common:3; Rare:91 | ||||
chr1:39026161-39026397 | Common:1; Rare:58 | ||||
chr1:39458986-39459215 | Common:2; Rare:58 | ||||
chr1:39691371-39691572 | Common:4; Rare:42 | ||||
chr1:39738724-39738903 | Common:2; Rare:35 | ||||
chr1:39883414-39883564 | Common:1; Rare:67; Clinvar (pathogenic):1 | ||||
chr1:40097216-40097343 | Common:1; Rare:56; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr1:40161231-40161409 | Common:1; Rare:48 | ||||
chr1:40257903-40258255 | Common:4; Rare:91; Clinvar:6 | ||||
chr1:40449827-40450167 | Common:5; Rare:122 | ||||
chr1:40508626-40508810 | Common:6; Rare:57 | ||||
chr1:40531514-40531649 | Rare:28 |