Variant report

Variant	rs10832842
Chromosome Location	chr11:17703136-17703137
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:17701946..17705746-chr11:17707792..17711044,3	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10766416	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10766420	0.94[EUR][1000 genomes]
rs10832845	0.88[EUR][1000 genomes]
rs10832851	0.85[EUR][1000 genomes]
rs10832852	0.85[EUR][1000 genomes]
rs11024384	0.85[EUR][1000 genomes]
rs11603216	0.85[EUR][1000 genomes]
rs11603221	0.85[EUR][1000 genomes]
rs12575678	0.98[ASN][1000 genomes]
rs12577406	0.92[ASN][1000 genomes]
rs12785437	0.84[EUR][1000 genomes]
rs16934638	1.00[ASN][1000 genomes]
rs17558336	0.92[ASN][1000 genomes]
rs2336849	0.85[EUR][1000 genomes]
rs28609365	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2878806	1.00[CEU][hapmap];0.85[CHB][hapmap];0.84[EUR][1000 genomes]
rs2878807	0.84[EUR][1000 genomes]
rs3858493	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858494	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858495	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858496	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858498	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858499	0.85[EUR][1000 genomes]
rs3858501	0.84[EUR][1000 genomes]
rs3858502	0.84[EUR][1000 genomes]
rs3858506	0.95[CEU][hapmap]
rs3858508	0.90[EUR][1000 genomes]
rs3890009	0.85[EUR][1000 genomes]
rs3901226	0.85[EUR][1000 genomes]
rs3901370	1.00[CEU][hapmap];0.85[CHB][hapmap];0.85[EUR][1000 genomes]
rs3911833	0.84[EUR][1000 genomes]
rs3928366	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4083362	0.85[EUR][1000 genomes]
rs4141262	0.94[ASN][1000 genomes]
rs4756912	0.95[CEU][hapmap]
rs4757568	0.85[CHB][hapmap]
rs4757569	0.85[CHB][hapmap]
rs4757570	0.95[CEU][hapmap]
rs61880586	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6416178	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6486390	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67265917	0.98[ASN][1000 genomes]
rs7106809	0.94[EUR][1000 genomes]
rs7107526	0.81[EUR][1000 genomes]
rs7109072	0.95[CEU][hapmap]
rs7128599	0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73420003	0.94[ASN][1000 genomes]
rs73420005	0.98[ASN][1000 genomes]
rs7478812	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7481960	0.86[ASN][1000 genomes]
rs7930233	0.80[EUR][1000 genomes]
rs7937727	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];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	nsv1040065	chr11:17556031-17753467	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1044126	chr11:17557715-17730646	Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv540953	chr11:17557715-17730646	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	esv2003029	chr11:17703075-17703476	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:17699200-17704000	Weak transcription	HSMM	muscle

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