Variant report

Variant	rs73371691
Chromosome Location	chr6:15152509-15152510
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:15143619..15146318-chr6:15151883..15153386,2	MCF-7	breast:
2	chr6:15106983..15108831-chr6:15151531..15154353,2	K562	blood:
3	chr6:15148839..15151214-chr6:15151716..15153395,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000264687	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs11968539	0.89[AFR][1000 genomes]
rs11968994	1.00[ASN][1000 genomes]
rs12524357	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12524540	1.00[ASN][1000 genomes]
rs12526221	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12527270	1.00[ASN][1000 genomes]
rs12527312	1.00[ASN][1000 genomes]
rs12528518	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12529010	1.00[ASN][1000 genomes]
rs12529719	1.00[ASN][1000 genomes]
rs12530015	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12530231	1.00[ASN][1000 genomes]
rs13193188	1.00[ASN][1000 genomes]
rs13193311	1.00[ASN][1000 genomes]
rs13204596	1.00[ASN][1000 genomes]
rs13213362	1.00[ASN][1000 genomes]
rs13220124	1.00[ASN][1000 genomes]
rs16876112	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1830498	0.95[AFR][1000 genomes]
rs28460493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34766885	1.00[ASN][1000 genomes]
rs35003605	1.00[ASN][1000 genomes]
rs57013338	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59109859	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61136001	1.00[ASN][1000 genomes]
rs61271709	1.00[ASN][1000 genomes]
rs6903057	0.80[AFR][1000 genomes]
rs6904999	1.00[ASN][1000 genomes]
rs6925982	0.80[AFR][1000 genomes]
rs6926190	1.00[ASN][1000 genomes]
rs6935098	0.80[AFR][1000 genomes]
rs73357717	1.00[ASN][1000 genomes]
rs73357719	1.00[ASN][1000 genomes]
rs73357720	1.00[ASN][1000 genomes]
rs73357732	1.00[ASN][1000 genomes]
rs73359689	1.00[ASN][1000 genomes]
rs73371668	0.91[AFR][1000 genomes]
rs73373408	0.82[AFR][1000 genomes]
rs73373422	0.89[AFR][1000 genomes]
rs73373423	0.89[AFR][1000 genomes]
rs73373435	0.89[AFR][1000 genomes]
rs73373441	0.89[AFR][1000 genomes]
rs73373454	0.80[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73375522	1.00[ASN][1000 genomes]
rs73375538	1.00[ASN][1000 genomes]
rs7742757	0.80[AFR][1000 genomes]
rs7746089	1.00[ASN][1000 genomes]
rs7771522	0.80[AFR][1000 genomes]
rs9464756	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9464758	1.00[ASN][1000 genomes]
rs9464759	1.00[ASN][1000 genomes]
rs9464760	1.00[ASN][1000 genomes]
rs9464772	1.00[ASN][1000 genomes]
rs9464775	1.00[ASN][1000 genomes]
rs9476767	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9476773	1.00[ASN][1000 genomes]
rs9476774	1.00[ASN][1000 genomes]
rs9476777	1.00[ASN][1000 genomes]
rs9476778	1.00[ASN][1000 genomes]
rs9476802	1.00[ASN][1000 genomes]
rs9718146	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016007	chr6:15099585-15159098	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2762580	chr6:15105917-15159110	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr6:15148600-15153000	Weak transcription	K562	blood
2	chr6:15149200-15153000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:15150400-15152600	Enhancers	Primary B cells from peripheral blood	blood
4	chr6:15150600-15152600	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr6:15152000-15153000	Weak transcription	Fetal Muscle Leg	muscle

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