Variant report

Variant rs58025793
Chromosome Location chr7:17310879-17310880
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17307600-17311200 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:17309400-17311000 ZNF genes & repeats Liver Liver
3 chr7:17309600-17311400 ZNF genes & repeats Dnd41 blood
4 chr7:17310000-17311000 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr7:17310000-17311000 ZNF genes & repeats Esophagus oesophagus
6 chr7:17310000-17311000 ZNF genes & repeats Fetal Lung lung
7 chr7:17310000-17311200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
8 chr7:17310000-17311200 Active TSS Fetal Heart heart
9 chr7:17310200-17311400 ZNF genes & repeats Fetal Intestine Small intestine
10 chr7:17310400-17311400 Weak transcription H9 Cell Line embryonic stem cell
11 chr7:17310600-17314000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr7:17310800-17311200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin03 Skin
13 chr7:17310800-17311400 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung

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