Variant report

Variant rs10510539
Chromosome Location chr3:23567468-23567469
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:23550800-23572000 Weak transcription Primary B cells from cord blood blood
2 chr3:23550800-23598600 Weak transcription HSMMtube muscle
3 chr3:23553000-23589600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr3:23561600-23570800 Weak transcription GM12878-XiMat blood
5 chr3:23565200-23572200 Weak transcription Primary B cells from peripheral blood blood
6 chr3:23567000-23568000 Enhancers HUVEC blood vessel
7 chr3:23567200-23567600 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr3:23567200-23568000 Enhancers HUES48 Cell Line embryonic stem cell
9 chr3:23567200-23568000 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr3:23567200-23568200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr3:23567200-23568600 Enhancers Brain Substantia Nigra brain
12 chr3:23567400-23568000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr3:23567400-23568000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr3:23567400-23568200 Enhancers HUES64 Cell Line embryonic stem cell
15 chr3:23567400-23568400 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
16 chr3:23567400-23589800 Weak transcription Psoas Muscle Psoas

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