Variant report

Variant	rs9493835
Chromosome Location	chr6:134438067-134438068
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:134416200-134438600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:134431400-134438600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:134434400-134438600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:134434600-134438600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr6:134436600-134438400	Weak transcription	Brain Anterior Caudate	brain
6	chr6:134436800-134438400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr6:134437000-134438400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:134437000-134438400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr6:134437200-134438400	Weak transcription	Brain Angular Gyrus	brain
10	chr6:134437200-134438400	Weak transcription	HSMM	muscle
11	chr6:134437400-134438400	Weak transcription	Brain Cingulate Gyrus	brain
12	chr6:134437400-134438600	Weak transcription	Brain Substantia Nigra	brain
13	chr6:134437600-134438400	Weak transcription	Brain Hippocampus Middle	brain
14	chr6:134438000-134438200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr6:134438000-134438600	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr6:134438000-134438800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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