Variant report

Variant rs502427
Chromosome Location chr11:86926738-86926739
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86882000-86928000 Weak transcription Left Ventricle heart
2 chr11:86891800-86929400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr11:86906000-86931000 Weak transcription Fetal Lung lung
4 chr11:86915400-86942000 Weak transcription HepG2 liver
5 chr11:86916000-86931000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr11:86924800-86934800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:86926400-86926800 Enhancers H1 Cell Line embryonic stem cell
8 chr11:86926400-86926800 ZNF genes & repeats Fetal Muscle Leg muscle
9 chr11:86926400-86926800 Enhancers K562 blood
10 chr11:86926600-86926800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr11:86926600-86926800 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr11:86926600-86926800 ZNF genes & repeats Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr11:86926600-86927000 Enhancers HUES48 Cell Line embryonic stem cell
14 chr11:86926600-86935200 Weak transcription Fetal Stomach stomach

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