Variant report

Variant rs566479956
Chromosome Location chr5:106982197-106982198
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:106969600-106988600 Weak transcription Fetal Stomach stomach
2 chr5:106970200-106985600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr5:106972200-106986000 Weak transcription HUES64 Cell Line embryonic stem cell
4 chr5:106972800-106983400 Weak transcription Fetal Lung lung
5 chr5:106976600-106984600 Weak transcription A549 lung
6 chr5:106976600-106987200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr5:106976600-106991600 Weak transcription Left Ventricle heart
8 chr5:106979200-106985800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr5:106979400-106985600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr5:106979400-106988600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr5:106981200-106982400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr5:106981200-106983800 Enhancers Pancreatic Islets Pancreatic Islet
13 chr5:106981600-106982200 Weak transcription Fetal Heart heart
14 chr5:106981600-106982400 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr5:106981600-106984400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr5:106981800-106982600 Enhancers NHEK skin
17 chr5:106981800-106985800 Weak transcription iPS-15b Cell Line embryonic stem cell
18 chr5:106982000-106982400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr5:106982000-106982600 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
20 chr5:106982000-106983400 Weak transcription HMEC breast

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