Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39565343-39565420 | Rare:17 | ||||
chr1:39569590-39569929 | Common:1; Rare:101 | ||||
chr1:39576257-39576402 | Rare:39 | ||||
chr1:39576632-39576907 | Rare:90 | ||||
chr1:39738748-39738927 | Common:2; Rare:45 | ||||
chr1:39883048-39883157 | Common:1; Rare:15 | ||||
chr1:39883345-39883624 | Common:1; Rare:108; Clinvar (pathogenic):1 | ||||
chr1:40040409-40040834 | Common:3; Rare:134 | ||||
chr1:40096612-40096685 | Common:1; Rare:15 | ||||
chr1:40097156-40097288 | Rare:61; Clinvar:5; Clinvar (benign):3; Clinvar (pathogenic):5 | ||||
chr1:40161255-40161405 | Rare:39 | ||||
chr1:40257897-40258392 | Common:4; Rare:143; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:40477163-40477325 | Common:3; Rare:49 | ||||
chr1:40508323-40508550 | Common:1; Rare:36 | ||||
chr1:40508653-40508894 | Common:4; Rare:62 |