Variant report

Variant	rs4598694
Chromosome Location	chr11:87334408-87334409
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 98 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs1010309	0.82[EUR][1000 genomes]
rs10501641	0.80[EUR][1000 genomes]
rs10501642	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10751172	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792974	0.83[EUR][1000 genomes]
rs10792975	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792976	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10792977	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898739	0.80[EUR][1000 genomes]
rs10898742	0.80[EUR][1000 genomes]
rs10898747	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898753	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10898754	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235221	0.80[EUR][1000 genomes]
rs11235224	0.82[EUR][1000 genomes]
rs11235225	0.82[EUR][1000 genomes]
rs11235237	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235245	0.89[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11235246	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11494293	0.80[EUR][1000 genomes]
rs11494294	0.80[EUR][1000 genomes]
rs11512889	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11600861	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11604094	0.80[EUR][1000 genomes]
rs11826467	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11826902	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11828839	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12278728	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12291846	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12291918	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12293810	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12361220	0.80[EUR][1000 genomes]
rs12362801	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12364147	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17150418	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17760207	0.80[EUR][1000 genomes]
rs1880116	0.80[EUR][1000 genomes]
rs2187330	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2212948	0.80[EUR][1000 genomes]
rs2212949	0.80[EUR][1000 genomes]
rs28370470	0.82[EUR][1000 genomes]
rs28702774	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28795771	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4245435	0.80[EUR][1000 genomes]
rs4278537	0.80[EUR][1000 genomes]
rs4284412	0.80[EUR][1000 genomes]
rs4463871	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4536254	0.80[EUR][1000 genomes]
rs4548644	0.81[EUR][1000 genomes]
rs4558186	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4622295	0.80[EUR][1000 genomes]
rs4627108	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4641508	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4943987	0.80[EUR][1000 genomes]
rs4944721	0.80[EUR][1000 genomes]
rs4944723	0.80[EUR][1000 genomes]
rs4944724	0.80[EUR][1000 genomes]
rs6592386	0.80[EUR][1000 genomes]
rs6592387	0.80[EUR][1000 genomes]
rs6592393	0.80[EUR][1000 genomes]
rs6592394	0.80[EUR][1000 genomes]
rs6592397	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6592402	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67701569	0.80[EUR][1000 genomes]
rs7105478	0.80[EUR][1000 genomes]
rs7114247	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7121065	0.80[EUR][1000 genomes]
rs7124539	0.80[EUR][1000 genomes]
rs7126228	0.80[EUR][1000 genomes]
rs7126694	0.82[EUR][1000 genomes]
rs7127253	0.80[EUR][1000 genomes]
rs72965688	0.80[EUR][1000 genomes]
rs72967546	0.82[EUR][1000 genomes]
rs72967550	0.82[EUR][1000 genomes]
rs7924614	0.80[EUR][1000 genomes]
rs7924814	0.80[EUR][1000 genomes]
rs7927078	0.80[EUR][1000 genomes]
rs7929162	0.80[EUR][1000 genomes]
rs7930759	0.82[EUR][1000 genomes]
rs7930765	0.80[EUR][1000 genomes]
rs7930820	0.80[EUR][1000 genomes]
rs7931538	0.80[EUR][1000 genomes]
rs7931854	0.80[EUR][1000 genomes]
rs7934337	0.80[EUR][1000 genomes]
rs7936294	0.80[EUR][1000 genomes]
rs7940053	0.82[EUR][1000 genomes]
rs7944286	0.80[EUR][1000 genomes]
rs7944779	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7947777	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7949528	0.80[EUR][1000 genomes]
rs9795164	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043562	chr11:86755535-87547185	Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv541120	chr11:86755535-87547185	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv555714	chr11:87058981-87399218	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1039172	chr11:87068731-87385458	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv832224	chr11:87162121-87355923	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv898075	chr11:87278074-87375119	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island	2 gene(s)	inside rSNPs	diseases
7	nsv555715	chr11:87307553-87349407	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region	1 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	chr11:87327800-87344600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:87334200-87334600	Enhancers	H1 Cell Line	embryonic stem cell
3	chr11:87334200-87334600	Enhancers	iPS-18 Cell Line	embryonic stem cell

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