Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:134485430-134485766 | Rare:80 | ||||
chr3:134485937-134486435 | Common:6; Rare:165 | ||||
chr3:136752341-136752684 | Common:1; Rare:111 | ||||
chr3:136861990-136862298 | Common:1; Rare:100 | ||||
chr3:138594209-138594447 | Rare:68 | ||||
chr3:139389530-139389864 | Common:2; Rare:108 | ||||
chr3:139539554-139540014 | Common:4; Rare:117 | ||||
chr3:141231665-141231890 | Common:2; Rare:79 | ||||
chr3:141368427-141368556 | Rare:29 | ||||
chr3:141402267-141402423 | Common:2; Rare:47 | ||||
chr3:141876014-141876168 | Rare:39 | ||||
chr3:141876453-141876670 | Common:1; Rare:82 | ||||
chr3:142225538-142225687 | Common:1; Rare:46 | ||||
chr3:142578707-142579011 | Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
chr3:143001351-143001631 | Common:4; Rare:95 |