Variant report

Variant rs138994308
Chromosome Location chr9:2699915-2699916
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:2688600-2702400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr9:2689800-2700200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr9:2690000-2702600 Weak transcription Primary T cells from cord blood blood
4 chr9:2690600-2718000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr9:2690800-2700600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr9:2691200-2710600 Weak transcription Left Ventricle heart
7 chr9:2692000-2709600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr9:2696600-2700600 Weak transcription ES-WA7 Cell Line embryonic stem cell
9 chr9:2697200-2722800 Weak transcription HSMM muscle
10 chr9:2698000-2717600 Weak transcription Esophagus oesophagus
11 chr9:2698200-2700400 Weak transcription Adipose Nuclei Adipose
12 chr9:2699000-2702200 Enhancers iPS-15b Cell Line embryonic stem cell
13 chr9:2699200-2701400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr9:2699400-2702200 Enhancers HUES64 Cell Line embryonic stem cell
15 chr9:2699600-2700400 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr9:2699800-2700000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
17 chr9:2699800-2700600 Enhancers iPS-18 Cell Line embryonic stem cell
18 chr9:2699800-2701000 Enhancers HUES48 Cell Line embryonic stem cell
19 chr9:2699800-2701600 Enhancers H1 Cell Line embryonic stem cell
20 chr9:2699800-2702000 Enhancers H9 Cell Line embryonic stem cell

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