Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10398734-10399097 | Common:2; Rare:129 | ||||
chr1:11262495-11262815 | Common:2; Rare:97 | ||||
chr1:11805935-11806255 | Common:2; Rare:86; Clinvar:1 | ||||
chr1:11934553-11934754 | Common:3; Rare:66; Clinvar:5; Clinvar (benign):1 | ||||
chr1:12617585-12617881 | Common:5; Rare:28 | ||||
chr1:12618207-12618397 | Rare:37 | ||||
chr1:15526603-15526917 | Common:2; Rare:101 | ||||
chr1:15758451-15758810 | Common:1; Rare:69 | ||||
chr1:16352420-16352587 | Common:3; Rare:88 | ||||
chr1:16980586-16980836 | Common:4; Rare:80 | ||||
chr1:17053997-17054317 | Common:3; Rare:96; Clinvar:5; Clinvar (benign):7 | ||||
chr1:19210254-19210503 | Rare:86 | ||||
chr1:19251512-19251866 | Common:6; Rare:115 | ||||
chr1:21176883-21177092 | Rare:46 | ||||
chr1:21345476-21345652 | Common:1; Rare:68 |