Variant report

Variant rs10489714
Chromosome Location chr1:185744111-185744112
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:185730200-185745000 Weak transcription Fetal Kidney kidney
2 chr1:185736000-185747000 Weak transcription Aorta Aorta
3 chr1:185737000-185744600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
4 chr1:185737800-185758800 Weak transcription Fetal Lung lung
5 chr1:185742800-185744400 Weak transcription Fetal Heart heart
6 chr1:185743200-185746000 Enhancers iPS-18 Cell Line embryonic stem cell
7 chr1:185743600-185744400 Enhancers iPS-20b Cell Line embryonic stem cell
8 chr1:185743600-185745000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr1:185743600-185745200 Enhancers HUES48 Cell Line embryonic stem cell
10 chr1:185743600-185747000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
11 chr1:185743800-185744800 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr1:185743800-185744800 Weak transcription HUES64 Cell Line embryonic stem cell
13 chr1:185743800-185745400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr1:185744000-185744600 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr1:185744000-185755000 Weak transcription iPS-15b Cell Line embryonic stem cell

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