Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:9942665-9942937 | Common:1; Rare:44 | ||||
chr1:9943272-9943507 | Common:2; Rare:69 | ||||
chr1:10032722-10033033 | Common:1; Rare:85 | ||||
chr1:10033377-10033590 | Common:2; Rare:33 | ||||
chr1:10398797-10399097 | Common:2; Rare:114 | ||||
chr1:10399316-10399468 | Common:3; Rare:32 | ||||
chr1:10430356-10430482 | Common:1; Rare:41 | ||||
chr1:11099722-11099918 | Common:2; Rare:79 | ||||
chr1:11189324-11189355 | Rare:7 | ||||
chr1:11262495-11262776 | Common:2; Rare:85 | ||||
chr1:11654417-11654530 | Rare:30 | ||||
chr1:11654712-11654938 | Common:4; Rare:59 | ||||
chr1:11805890-11806265 | Common:2; Rare:106; Clinvar:1 | ||||
chr1:11980081-11980495 | Common:6; Rare:130; Clinvar:1; Clinvar (benign):5 | ||||
chr1:12229978-12230113 | Common:1; Rare:45 |