Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:15197897-15197923 | Rare:6 | ||||
chr1:15718482-15718613 | Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
chr1:15721186-15721384 | Common:1; Rare:42 | ||||
chr1:15725015-15725474 | Common:4; Rare:142; Clinvar (benign):2 | ||||
chr1:15800233-15800407 | Rare:32 | ||||
chr1:15834872-15835133 | Common:2; Rare:116 | ||||
chr1:15835840-15836097 | Common:6; Rare:114 | ||||
chr1:16155109-16155261 | Common:1; Rare:25 | ||||
chr1:16458631-16458915 | Common:1; Rare:64 | ||||
chr1:16620042-16620348 | Common:5; Rare:6 | ||||
chr1:16644610-16644789 | Common:1; Rare:2 | ||||
chr1:16645475-16645622 | Common:2; Rare:2 | ||||
chr1:16696778-16696863 | Rare:42 | ||||
chr1:16697238-16697505 | Common:2; Rare:21 | ||||
chr1:16889642-16889706 | Common:1; Rare:17 |