Variant report

Variant	rs12775838
Chromosome Location	chr10:27573707-27573708
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:27531276..27533998-chr10:27572512..27575307,2	K562	blood:

Variant related genes	Relation type
ENSG00000262412	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10829217	0.88[ASN][1000 genomes]
rs10829218	0.89[ASN][1000 genomes]
rs11015624	0.88[ASN][1000 genomes]
rs11015628	0.94[ASN][1000 genomes]
rs11812283	0.88[ASN][1000 genomes]
rs11812740	0.88[ASN][1000 genomes]
rs11818418	1.00[ASN][1000 genomes]
rs12260818	1.00[ASN][1000 genomes]
rs12262209	1.00[ASN][1000 genomes]
rs12264871	0.82[ASN][1000 genomes]
rs12415447	0.82[ASN][1000 genomes]
rs12774718	0.88[ASN][1000 genomes]
rs12775195	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12775266	0.81[AMR][1000 genomes]
rs12778080	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16916444	0.82[ASN][1000 genomes]
rs17476860	0.84[AMR][1000 genomes]
rs17476874	0.84[AMR][1000 genomes]
rs17748862	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1930960	1.00[ASN][1000 genomes]
rs2027538	0.88[ASN][1000 genomes]
rs34544855	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34983424	1.00[ASN][1000 genomes]
rs35053986	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35931272	1.00[ASN][1000 genomes]
rs3864846	0.81[AMR][1000 genomes]
rs4747592	0.88[ASN][1000 genomes]
rs4747594	0.88[ASN][1000 genomes]
rs55770293	1.00[ASN][1000 genomes]
rs56207199	1.00[ASN][1000 genomes]
rs56313380	1.00[ASN][1000 genomes]
rs56406502	1.00[ASN][1000 genomes]
rs57002554	0.84[AMR][1000 genomes]
rs59575776	0.84[AMR][1000 genomes]
rs61149145	0.88[ASN][1000 genomes]
rs67395401	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73598052	0.94[ASN][1000 genomes]
rs7918793	0.88[ASN][1000 genomes]
rs7919198	0.88[ASN][1000 genomes]
rs7919807	0.88[ASN][1000 genomes]
rs7920681	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422253	chr10:27431366-27575370	Strong transcription Genic enhancers Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	esv3337781	chr10:27472216-27666703	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv8614	chr10:27504487-27828406	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv550241	chr10:27569521-28025771	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
5	esv3413607	chr10:27569733-27577795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1045257	chr10:27572440-27926946	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:27573200-27574200	Enhancers	Liver	Liver

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