Variant report

Variant	rs6760968
Chromosome Location	chr2:213302836-213302837
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10207963	1.00[ASN][1000 genomes]
rs11695241	0.97[ASN][1000 genomes]
rs13422701	0.97[ASN][1000 genomes]
rs16848583	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16848584	0.97[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1813049	0.97[ASN][1000 genomes]
rs2170530	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6435706	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6710782	1.00[ASN][1000 genomes]
rs6715328	0.97[ASN][1000 genomes]
rs6752016	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73989003	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs73989006	1.00[ASN][1000 genomes]
rs73989011	1.00[ASN][1000 genomes]
rs73989012	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73989013	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7570124	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7593163	1.00[ASN][1000 genomes]
rs7603379	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834527	chr2:213115966-213334308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
2	nsv1004573	chr2:213186537-213365252	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
3	nsv875811	chr2:213200920-213347104	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA	2 gene(s)	inside rSNPs	diseases
4	esv34076	chr2:213298576-213306627	Weak transcription Enhancers	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:213302000-213306600	Weak transcription	Aorta	Aorta

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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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