Variant report

Variant	rs1112718
Chromosome Location	chr10:94479107-94479108
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10748582	0.93[EUR][1000 genomes]
rs10786053	0.93[EUR][1000 genomes]
rs10882104	0.93[EUR][1000 genomes]
rs10882105	0.93[EUR][1000 genomes]
rs10882106	0.93[EUR][1000 genomes]
rs11187140	0.90[EUR][1000 genomes]
rs11187141	0.93[EUR][1000 genomes]
rs11187143	0.93[EUR][1000 genomes]
rs11187144	0.94[EUR][1000 genomes]
rs11187149	0.93[EUR][1000 genomes]
rs1544210	0.83[ASN][1000 genomes]
rs1832886	0.93[EUR][1000 genomes]
rs2488075	0.87[ASN][1000 genomes]
rs2497306	0.86[ASN][1000 genomes]
rs2901609	0.86[EUR][1000 genomes]
rs34744311	0.87[EUR][1000 genomes]
rs4933736	0.93[EUR][1000 genomes]
rs7087591	0.94[EUR][1000 genomes]
rs7898054	0.93[EUR][1000 genomes]
rs7923837	0.92[EUR][1000 genomes]
rs7923866	0.93[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	esv3446249	chr10:94374508-94549394	Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94471200-94481200	Enhancers	Primary B cells from peripheral blood	blood
2	chr10:94475800-94480400	Weak transcription	Spleen	Spleen
3	chr10:94477000-94486600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:94477200-94482600	Weak transcription	Pancreas	Pancrea
5	chr10:94479000-94481200	Enhancers	Primary B cells from cord blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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