Variant report

Variant rs35667895
Chromosome Location chr2:180511158-180511159
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180502400-180511600 Weak transcription Fetal Heart heart
2 chr2:180506800-180511200 Weak transcription Fetal Brain Female brain
3 chr2:180508400-180517000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr2:180510200-180511200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr2:180510200-180512200 Enhancers Fetal Lung lung
6 chr2:180510200-180512400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr2:180510400-180511400 Enhancers HepG2 liver
8 chr2:180510600-180513600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr2:180511000-180512200 Enhancers Liver Liver
10 chr2:180511000-180513200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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