Variant report

Variant	rs10761278
Chromosome Location	chr9:96566975-96566976
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10156579	0.81[EUR][1000 genomes]
rs10761263	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10761276	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10761277	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10761279	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10761280	0.85[EUR][1000 genomes]
rs10821224	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10821225	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10821226	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10821227	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10821239	0.80[EUR][1000 genomes]
rs10992905	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12000834	0.85[EUR][1000 genomes]
rs4604507	0.81[EUR][1000 genomes]
rs4744288	0.81[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96563800-96569400	Weak transcription	K562	blood
2	chr9:96564400-96569400	Weak transcription	iPS DF 19.11 Cell Line	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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