Variant report

Variant	rs546193684
Chromosome Location	chr11:83218162-83218163
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3343792	chr11:83217704-83219852	Enhancers Weak transcription Active TSS	n/a	n/a	inside rSNPs	n/a
2	esv3437429	chr11:83218154-83219502	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83211400-83220000	Weak transcription	Brain Angular Gyrus	brain
2	chr11:83211600-83219000	Weak transcription	Brain Substantia Nigra	brain
3	chr11:83211600-83222200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr11:83214000-83219400	Weak transcription	Fetal Intestine Large	intestine
5	chr11:83215800-83219600	Weak transcription	Liver	Liver
6	chr11:83215800-83219600	Weak transcription	Fetal Intestine Small	intestine
7	chr11:83218000-83221600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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