Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:105013563-105013652 | Rare:30 | ||||
chr7:105639119-105639320 | Common:2; Rare:34 | ||||
chr7:107661687-107661893 | Rare:80; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):6 | ||||
chr7:112205590-112205646 | Rare:15 | ||||
chr7:113118549-113118664 | Common:1; Rare:37 | ||||
chr7:116211462-116211568 | Rare:22 | ||||
chr7:131106351-131106458 | Rare:24 | ||||
chr7:131108089-131108187 | Rare:14 | ||||
chr7:141072335-141072641 | Common:1; Rare:55 | ||||
chr7:148983525-148983755 | Common:3; Rare:90 | ||||
chr7:148987246-148987527 | Common:8; Rare:90 | ||||
chr7:152436520-152436864 | Rare:117 | ||||
chr8:9903396-9903618 | Rare:52 | ||||
chr8:9903717-9903763 | Rare:10 | ||||
chr8:9904162-9904533 | Common:3; Rare:114 |