Variant report

Variant rs537980179
Chromosome Location chr1:169227170-169227171
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169220000-169229800 Weak transcription HUVEC blood vessel
2 chr1:169220600-169230000 Weak transcription Liver Liver
3 chr1:169224800-169227400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr1:169225000-169229800 Weak transcription Primary T cells from cord blood blood
5 chr1:169226400-169227400 ZNF genes & repeats Fetal Stomach stomach
6 chr1:169226400-169227600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr1:169226400-169227600 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
8 chr1:169226400-169227600 ZNF genes & repeats Fetal Intestine Small intestine
9 chr1:169226800-169228200 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr1:169227000-169227600 ZNF genes & repeats Primary B cells from cord blood blood
11 chr1:169227000-169227600 ZNF genes & repeats Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:169227000-169227600 Strong transcription Fetal Kidney kidney
13 chr1:169227000-169228400 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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