Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:46604044-46604493 | Common:3; Rare:123 | ||||
chr1:46616610-46616922 | Common:3; Rare:63 | ||||
chr1:46667961-46668131 | Rare:53 | ||||
chr1:46668311-46668594 | Common:2; Rare:88 | ||||
chr1:46719075-46719345 | Rare:103 | ||||
chr1:46806854-46806884 | Rare:6 | ||||
chr1:47190292-47190459 | Common:1; Rare:25 | ||||
chr1:47190939-47191224 | Common:1; Rare:46 | ||||
chr1:47191483-47191880 | Rare:57 | ||||
chr1:47231826-47231980 | Common:1; Rare:30 | ||||
chr1:47232163-47232257 | Rare:26 | ||||
chr1:47232266-47232427 | Rare:35 | ||||
chr1:47232545-47232597 | Rare:4 | ||||
chr1:47313521-47313774 | Common:1; Rare:37 | ||||
chr1:47313993-47314776 | Common:6; Rare:157; Clinvar:3; Clinvar (benign):1 |