Variant report

Variant rs11099032
Chromosome Location chr4:131002156-131002157
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:130995600-131002200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr4:130995600-131005000 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr4:130999800-131007000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr4:131000600-131002200 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr4:131001400-131002600 Enhancers Fetal Intestine Small intestine
6 chr4:131001600-131002400 Enhancers Stomach Mucosa stomach
7 chr4:131001600-131002600 Enhancers Liver Liver
8 chr4:131001600-131002600 Enhancers Duodenum Mucosa Duodenum
9 chr4:131001600-131002600 Enhancers Fetal Intestine Large intestine
10 chr4:131002000-131002400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr4:131002000-131002400 Enhancers NHEK skin
12 chr4:131002000-131002600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr4:131002000-131002600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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