Variant report

Variant	rs6751197
Chromosome Location	chr2:205088743-205088744
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11891596	1.00[EUR][1000 genomes]
rs16824667	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2216958	1.00[EUR][1000 genomes]
rs6709185	1.00[EUR][1000 genomes]
rs6751909	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6752041	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

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	nsv518928	chr2:205084439-205090645	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205086600-205090800	Weak transcription	Aorta	Aorta
2	chr2:205087400-205089600	Enhancers	Fetal Muscle Leg	muscle
3	chr2:205088200-205088800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr2:205088200-205088800	Enhancers	Gastric	stomach
5	chr2:205088400-205092800	Weak transcription	Fetal Brain Female	brain
6	chr2:205088400-205093200	Enhancers	Brain Germinal Matrix	brain

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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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