Variant report

Variant	rs60962878
Chromosome Location	chr8:60940539-60940540
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10092264	0.89[AFR][1000 genomes]
rs10104844	0.88[AFR][1000 genomes]
rs10105249	0.86[AFR][1000 genomes]
rs10113409	0.89[AFR][1000 genomes]
rs11986881	0.95[AFR][1000 genomes]
rs11988688	1.00[EUR][1000 genomes]
rs11990259	0.98[AFR][1000 genomes]
rs11997353	0.98[AFR][1000 genomes]
rs13439744	0.85[AFR][1000 genomes]
rs16925559	0.91[AFR][1000 genomes]
rs16925586	1.00[EUR][1000 genomes]
rs17280265	0.89[AFR][1000 genomes]
rs17280286	0.87[AFR][1000 genomes]
rs17280386	0.87[AFR][1000 genomes]
rs17280559	0.91[AFR][1000 genomes]
rs17280832	0.93[AFR][1000 genomes]
rs17281312	0.93[AFR][1000 genomes]
rs17346051	0.89[AFR][1000 genomes]
rs17346319	0.95[AFR][1000 genomes]
rs17346443	0.91[AFR][1000 genomes]
rs17346637	0.86[AFR][1000 genomes]
rs28429790	0.89[AFR][1000 genomes]
rs28483493	0.98[AFR][1000 genomes]
rs28654982	0.91[AFR][1000 genomes]
rs57683092	1.00[EUR][1000 genomes]
rs59240261	1.00[EUR][1000 genomes]
rs59361057	1.00[EUR][1000 genomes]
rs60478918	1.00[EUR][1000 genomes]
rs62512128	0.89[AFR][1000 genomes]
rs62512129	0.83[AFR][1000 genomes]
rs62512130	0.98[AFR][1000 genomes]
rs62512131	0.98[AFR][1000 genomes]
rs62512132	0.91[AFR][1000 genomes]
rs73682244	0.87[AFR][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	nsv831331	chr8:60770382-60959633	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60939800-60943000	Weak transcription	Primary B cells from cord blood	blood
2	chr8:60940000-60942400	Weak transcription	Primary B cells from peripheral blood	blood
3	chr8:60940000-60968400	Weak transcription	H1 BMP4 Derived Mesendoderm 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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