Variant report

Variant rs35721293
Chromosome Location chr5:178256761-178256762
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:178253200-178257000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr5:178253200-178257800 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr5:178254000-178259400 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr5:178254200-178259400 Weak transcription iPS-15b Cell Line embryonic stem cell
5 chr5:178254400-178258200 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr5:178254600-178256800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr5:178255000-178257000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr5:178255800-178257200 Enhancers H9 Cell Line embryonic stem cell
9 chr5:178255800-178257200 Bivalent Enhancer Fetal Brain Male brain
10 chr5:178255800-178257600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr5:178256000-178256800 Enhancers Adipose Nuclei Adipose
12 chr5:178256000-178257200 Enhancers ES-I3 Cell Line embryonic stem cell
13 chr5:178256400-178257200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr5:178256400-178258600 Weak transcription iPS-20b Cell Line embryonic stem cell
15 chr5:178256600-178257000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
16 chr5:178256600-178258200 Weak transcription K562 blood

Quick Search:


  
Input of quick search could be:

what's new

Quick links