Variant report

Variant	rs12262082
Chromosome Location	chr10:26969524-26969525
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:26968705..26971277-chr10:26973238..26975564,2	K562	blood:
2	chr10:26958878..26961575-chr10:26966609..26969572,2	K562	blood:
3	chr10:26965108..26970102-chr10:26984839..26987979,6	K562	blood:
4	chr10:26965218..26966801-chr10:26966890..26969574,2	K562	blood:

Variant related genes	Relation type
ENSG00000148459	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10128125	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10128192	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10829048	1.00[ASN][1000 genomes]
rs11015219	1.00[AFR][1000 genomes]
rs11015220	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015226	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11015230	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11015233	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11015234	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11816510	0.83[ASN][1000 genomes]
rs11818450	0.83[ASN][1000 genomes]
rs12242239	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12242414	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12245051	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12246285	1.00[ASN][1000 genomes]
rs12247299	1.00[ASN][1000 genomes]
rs12247597	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12252298	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12252358	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12252368	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12255583	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12255942	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260035	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12260298	1.00[ASN][1000 genomes]
rs12260466	0.96[ASN][1000 genomes]
rs12262401	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263262	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263578	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12264509	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12265505	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12265633	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12265746	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12267744	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12268883	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12269520	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17754039	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17754051	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1980754	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2005120	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2477276	0.81[ASN][1000 genomes]
rs2489564	0.81[ASN][1000 genomes]
rs34314417	0.96[ASN][1000 genomes]
rs34901510	1.00[ASN][1000 genomes]
rs35534478	1.00[ASN][1000 genomes]
rs35687107	1.00[ASN][1000 genomes]
rs35827769	1.00[ASN][1000 genomes]
rs4309054	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7097696	1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs72485013	0.94[ASN][1000 genomes]
rs72485015	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485017	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485018	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485022	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72485023	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72485026	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs753705	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7899631	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7900674	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7906473	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7920279	0.94[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[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	nsv894975	chr10:26343356-27014467	Strong transcription Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	nsv1044057	chr10:26894348-26971879	Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3333006	chr10:26908323-26985227	Bivalent Enhancer Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv3415799	chr10:26929831-27233591	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
5	esv1798973	chr10:26968171-27001814	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv550233	chr10:26968171-27011323	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:26967000-26973800	Weak transcription	K562	blood
2	chr10:26969400-26969800	ZNF genes & repeats	Fetal Thymus	thymus
3	chr10:26969400-26969800	Enhancers	Thymus	Thymus
4	chr10:26969400-26972200	Enhancers	Primary monocytes fromperipheralblood	blood

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