Variant report

Variant	rs11503871
Chromosome Location	chr12:48352248-48352249
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11168330	0.82[AFR][1000 genomes]
rs11168331	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11503872	0.82[AFR][1000 genomes]
rs11503873	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12313208	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12318838	0.82[AFR][1000 genomes]
rs12721425	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12721426	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12721427	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1541408	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2408878	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35000511	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41272749	0.90[EUR][1000 genomes]
rs41272777	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56196515	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7135926	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73297161	0.82[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	nsv832401	chr12:48347453-48477999	Weak transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:48351800-48353000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
2	chr12:48352200-48352400	ZNF genes & repeats	iPS-20b 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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