Variant report

Variant	rs184649503
Chromosome Location	chr11:83339773-83339774
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3347751	chr11:83339741-83339881	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83324200-83341200	Weak transcription	Brain Anterior Caudate	brain
2	chr11:83324400-83340400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr11:83335800-83340200	Weak transcription	Brain Substantia Nigra	brain
4	chr11:83336200-83340400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr11:83339400-83340000	Enhancers	NHEK	skin
6	chr11:83339600-83339800	Enhancers	Brain Hippocampus Middle	brain
7	chr11:83339600-83340000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr11:83339600-83341800	Enhancers	Fetal Brain Male	brain

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

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