Variant report

Variant rs11590708
Chromosome Location chr1:57819267-57819268
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:57800000-57826600 Weak transcription Left Ventricle heart
2 chr1:57808200-57822400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr1:57814600-57819400 Weak transcription Lung lung
4 chr1:57816400-57822800 Weak transcription H9 Cell Line embryonic stem cell
5 chr1:57817600-57822400 Weak transcription Fetal Brain Female brain
6 chr1:57817600-57826600 Weak transcription Fetal Brain Male brain
7 chr1:57818800-57819400 Enhancers Fetal Stomach stomach
8 chr1:57819000-57819400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
9 chr1:57819000-57819400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr1:57819000-57819400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:57819000-57819400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr1:57819000-57819400 Active TSS Spleen Spleen
13 chr1:57819000-57819800 Enhancers Fetal Lung lung
14 chr1:57819200-57819400 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr1:57819200-57819400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
16 chr1:57819200-57821400 Enhancers Fetal Heart heart

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