Variant report

Variant rs7115293
Chromosome Location chr11:86996762-86996763
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86991600-87014200 Weak transcription HepG2 liver
2 chr11:86992000-87017600 Weak transcription Aorta Aorta
3 chr11:86992600-87020600 Weak transcription Liver Liver
4 chr11:86993000-87001600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr11:86993200-87009000 Weak transcription HUVEC blood vessel
6 chr11:86994000-87014200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr11:86995200-87018800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr11:86995400-86996800 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr11:86995600-86999800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr11:86995800-87007200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr11:86996400-86996800 ZNF genes & repeats iPS DF 6.9 Cell Line embryonic stem cell
12 chr11:86996400-86996800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
13 chr11:86996400-86997800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
14 chr11:86996600-86996800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr11:86996600-86996800 ZNF genes & repeats iPS-15b Cell Line embryonic stem cell
16 chr11:86996600-86996800 ZNF genes & repeats K562 blood

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