Variant report

Variant rs1093510
Chromosome Location chr13:38489369-38489370
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:38484200-38494200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr13:38488200-38494200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
3 chr13:38488400-38491000 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr13:38488600-38489600 ZNF genes & repeats iPS-18 Cell Line embryonic stem cell
5 chr13:38488800-38489400 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
6 chr13:38488800-38489800 Enhancers HMEC breast
7 chr13:38488800-38489800 ZNF genes & repeats NHEK skin
8 chr13:38489000-38489400 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr13:38489000-38489400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr13:38489200-38489400 Flanking Active TSS HUES48 Cell Line embryonic stem cell
11 chr13:38489200-38489400 Active TSS iPS-20b Cell Line embryonic stem cell
12 chr13:38489200-38489400 ZNF genes & repeats Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr13:38489200-38491000 Active TSS H9 Cell Line embryonic stem cell
14 chr13:38489200-38492200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
15 chr13:38489200-38492400 Active TSS H1 Cell Line embryonic stem cell
16 chr13:38489200-38494000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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