Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193115699-193115896 | Rare:41 | ||||
chr1:196404227-196404476 | Common:1; Rare:39 | ||||
chr1:197201238-197201543 | Common:1; Rare:105 | ||||
chr1:200738724-200738961 | Common:6; Rare:73 | ||||
chr1:202861524-202861751 | Common:1; Rare:63 | ||||
chr1:203627951-203628057 | Rare:16 | ||||
chr1:211382733-211382858 | Common:1; Rare:52 | ||||
chr1:223992554-223992789 | Common:4; Rare:87 | ||||
chr1:244863774-244863836 | Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
chr1:247210815-247210890 | Rare:28 | ||||
chr10:5596080-5596373 | Common:1; Rare:56 | ||||
chr10:5945896-5946038 | Common:7; Rare:41 | ||||
chr10:6163634-6163869 | Common:6; Rare:79 | ||||
chr10:13891697-13891970 | Common:3; Rare:78 | ||||
chr10:17023494-17023650 | Rare:35 |