Variant report

Variant rs9493824
Chromosome Location chr6:134401812-134401813
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:134395600-134405000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr6:134396800-134402800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
3 chr6:134398800-134404200 Enhancers Placenta Placenta
4 chr6:134400000-134402000 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr6:134400200-134404600 Enhancers Primary B cells from cord blood blood
6 chr6:134400200-134404600 Enhancers Primary B cells from peripheral blood blood
7 chr6:134400600-134402000 Enhancers NHEK skin
8 chr6:134401000-134402200 Enhancers Primary T helper cells PMA-I stimulated --
9 chr6:134401400-134402200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr6:134401400-134402600 Weak transcription HUES64 Cell Line embryonic stem cell
11 chr6:134401600-134402000 Enhancers Hela-S3 cervix
12 chr6:134401800-134402200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
13 chr6:134401800-134403200 Weak transcription GM12878-XiMat blood

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