Variant report

Variant rs534381927
Chromosome Location chr9:2692265-2692266
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:2679400-2692400 Weak transcription Psoas Muscle Psoas
2 chr9:2687200-2693200 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr9:2688600-2702400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr9:2689800-2700200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr9:2690000-2692600 Enhancers HUVEC blood vessel
6 chr9:2690000-2702600 Weak transcription Primary T cells from cord blood blood
7 chr9:2690600-2718000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
8 chr9:2690800-2700600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr9:2691200-2710600 Weak transcription Left Ventricle heart
10 chr9:2691400-2692600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr9:2692000-2709600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr9:2692200-2693200 Weak transcription Fetal Heart heart

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