Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26279934-26280203 | Rare:144 | ||||
chr1:26432091-26432403 | Common:5; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472279-26472524 | Common:4; Rare:78 | ||||
chr1:26787870-26788207 | Common:3; Rare:94; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26900423-26900547 | Rare:45 | ||||
chr1:27322052-27322316 | Common:1; Rare:94 | ||||
chr1:27725762-27725996 | Common:2; Rare:62 | ||||
chr1:27772903-27773291 | Common:1; Rare:123 | ||||
chr1:27830618-27830837 | Common:3; Rare:71 | ||||
chr1:28232953-28233082 | Common:1; Rare:55 | ||||
chr1:28328894-28329073 | Common:1; Rare:57 | ||||
chr1:28505801-28506062 | Common:2; Rare:100 | ||||
chr1:28552882-28553120 | Common:2; Rare:91 | ||||
chr1:28643012-28643197 | Rare:71 | ||||
chr1:28668667-28668830 | Common:1; Rare:56 |