Variant report

Variant	rs1819081
Chromosome Location	chr7:84499593-84499594
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:84165204..84166004-chr7:84499385..84500020,2	MCF-7	breast:
2	chr7:84165144..84166088-chr7:84499191..84500054,5	MCF-7	breast:
3	chr7:84498615..84500750-chr7:84525204..84526941,2	K562	blood:
4	chr7:84498248..84502734-chr7:84505735..84508151,4	K562	blood:
5	chr7:84158432..84159358-chr7:84499153..84500086,4	MCF-7	breast:
6	chr7:84158432..84159047-chr7:84499527..84500086,2	MCF-7	breast:
7	chr7:84474585..84476459-chr7:84497349..84500162,2	K562	blood:
8	chr7:84165588..84166207-chr7:84499370..84499987,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000232605	Chromatin interaction

Extended variants
information (count: 155 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:151)

rs_ID	r²[population]
rs10085515	0.95[CEU][hapmap];0.97[GIH][hapmap];0.91[TSI][hapmap];0.91[EUR][1000 genomes]
rs10224730	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10225306	0.89[EUR][1000 genomes]
rs10226150	0.89[EUR][1000 genomes]
rs10227116	0.89[EUR][1000 genomes]
rs10229754	0.89[EUR][1000 genomes]
rs10232046	0.82[EUR][1000 genomes]
rs10235869	0.83[EUR][1000 genomes]
rs10239803	0.87[EUR][1000 genomes]
rs10240021	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10243996	0.83[EUR][1000 genomes]
rs10246917	0.87[EUR][1000 genomes]
rs10249026	0.87[EUR][1000 genomes]
rs10260931	0.87[EUR][1000 genomes]
rs10265300	0.83[EUR][1000 genomes]
rs10272662	0.90[EUR][1000 genomes]
rs10274330	0.87[EUR][1000 genomes]
rs1030539	0.87[EUR][1000 genomes]
rs1030540	0.89[EUR][1000 genomes]
rs1030541	0.87[EUR][1000 genomes]
rs10954760	0.90[CEU][hapmap];0.91[GIH][hapmap];0.91[TSI][hapmap];0.82[EUR][1000 genomes]
rs10954761	0.84[EUR][1000 genomes]
rs1118915	0.87[EUR][1000 genomes]
rs11761247	0.90[CEU][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.83[EUR][1000 genomes]
rs11764839	0.85[EUR][1000 genomes]
rs11765826	0.87[EUR][1000 genomes]
rs11976179	0.83[EUR][1000 genomes]
rs11980701	0.91[EUR][1000 genomes]
rs11981981	0.85[EUR][1000 genomes]
rs12154861	0.87[EUR][1000 genomes]
rs12155118	0.87[EUR][1000 genomes]
rs12155210	0.83[EUR][1000 genomes]
rs12672643	0.90[CEU][hapmap];0.91[GIH][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes]
rs12707673	0.82[EUR][1000 genomes]
rs12707677	0.82[EUR][1000 genomes]
rs12707680	0.84[EUR][1000 genomes]
rs12707681	0.88[EUR][1000 genomes]
rs12707682	0.89[EUR][1000 genomes]
rs12707683	0.89[EUR][1000 genomes]
rs12707684	0.87[EUR][1000 genomes]
rs13221551	0.87[EUR][1000 genomes]
rs13225076	0.87[EUR][1000 genomes]
rs13226061	0.85[EUR][1000 genomes]
rs13227983	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13235916	0.87[EUR][1000 genomes]
rs13239654	0.87[EUR][1000 genomes]
rs13240109	0.92[EUR][1000 genomes]
rs13243442	0.87[EUR][1000 genomes]
rs13243701	0.85[EUR][1000 genomes]
rs13244454	0.82[EUR][1000 genomes]
rs13247373	0.82[EUR][1000 genomes]
rs13340534	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1430593	0.94[EUR][1000 genomes]
rs1579511	0.83[EUR][1000 genomes]
rs1583135	0.86[EUR][1000 genomes]
rs1583136	0.89[EUR][1000 genomes]
rs1583137	0.90[EUR][1000 genomes]
rs1583142	0.87[EUR][1000 genomes]
rs1583143	0.80[EUR][1000 genomes]
rs1583144	0.87[EUR][1000 genomes]
rs1583145	0.87[EUR][1000 genomes]
rs1583147	0.89[EUR][1000 genomes]
rs1594388	0.87[EUR][1000 genomes]
rs1594390	0.87[EUR][1000 genomes]
rs1594392	0.90[CEU][hapmap];0.89[EUR][1000 genomes]
rs1594393	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1599876	0.87[EUR][1000 genomes]
rs1599877	0.87[EUR][1000 genomes]
rs1599878	0.87[EUR][1000 genomes]
rs1609872	0.87[EUR][1000 genomes]
rs1609875	0.87[EUR][1000 genomes]
rs1609876	0.89[EUR][1000 genomes]
rs1609877	0.87[EUR][1000 genomes]
rs1813781	0.89[EUR][1000 genomes]
rs1820960	0.87[EUR][1000 genomes]
rs1820961	0.88[EUR][1000 genomes]
rs1820962	0.87[EUR][1000 genomes]
rs1835403	0.87[EUR][1000 genomes]
rs1897151	0.87[EUR][1000 genomes]
rs1897155	0.87[EUR][1000 genomes]
rs1897158	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1919284	0.94[EUR][1000 genomes]
rs1919285	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1919287	0.95[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1961063	0.95[CEU][hapmap];0.89[EUR][1000 genomes]
rs1963873	0.87[EUR][1000 genomes]
rs1965737	0.87[EUR][1000 genomes]
rs1982016	0.86[EUR][1000 genomes]
rs1982019	0.81[EUR][1000 genomes]
rs1982020	0.87[EUR][1000 genomes]
rs1984778	0.84[EUR][1000 genomes]
rs1988767	0.87[EUR][1000 genomes]
rs1997303	0.90[EUR][1000 genomes]
rs2099203	0.87[EUR][1000 genomes]
rs2141416	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2195647	0.94[EUR][1000 genomes]
rs2195648	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2217453	0.92[EUR][1000 genomes]
rs28613865	0.87[EUR][1000 genomes]
rs28671173	0.87[EUR][1000 genomes]
rs34085748	0.81[EUR][1000 genomes]
rs34701264	0.89[EUR][1000 genomes]
rs34905624	0.87[EUR][1000 genomes]
rs35037906	0.91[EUR][1000 genomes]
rs35169726	0.87[EUR][1000 genomes]
rs35433276	0.80[EUR][1000 genomes]
rs35508218	0.90[EUR][1000 genomes]
rs35992683	0.90[EUR][1000 genomes]
rs3886737	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4301393	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4395839	0.90[CEU][hapmap];0.91[GIH][hapmap];0.91[TSI][hapmap];0.87[EUR][1000 genomes]
rs4401790	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4481537	0.89[EUR][1000 genomes]
rs4503051	0.83[EUR][1000 genomes]
rs4518607	0.95[CEU][hapmap];0.97[GIH][hapmap];0.97[TSI][hapmap];0.93[EUR][1000 genomes]
rs4534087	0.91[EUR][1000 genomes]
rs4563833	0.95[CEU][hapmap];0.97[GIH][hapmap];0.91[TSI][hapmap];0.89[EUR][1000 genomes]
rs4728560	0.83[EUR][1000 genomes]
rs58730623	0.87[EUR][1000 genomes]
rs62471868	0.83[EUR][1000 genomes]
rs62474471	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62474473	0.87[EUR][1000 genomes]
rs62474474	0.87[EUR][1000 genomes]
rs62474475	0.87[EUR][1000 genomes]
rs62474492	0.87[EUR][1000 genomes]
rs6468002	0.87[EUR][1000 genomes]
rs6468003	0.87[EUR][1000 genomes]
rs6468004	0.87[EUR][1000 genomes]
rs6946368	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs71560704	0.95[EUR][1000 genomes]
rs732793	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs732794	0.89[EUR][1000 genomes]
rs732795	0.89[EUR][1000 genomes]
rs733513	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs752660	0.89[EUR][1000 genomes]
rs752664	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7777318	0.89[EUR][1000 genomes]
rs7782136	0.87[EUR][1000 genomes]
rs7782980	0.87[EUR][1000 genomes]
rs7783653	0.83[EUR][1000 genomes]
rs7787961	0.82[EUR][1000 genomes]
rs7799648	0.95[CEU][hapmap];0.97[GIH][hapmap];0.91[TSI][hapmap];0.93[EUR][1000 genomes]
rs7801827	0.87[EUR][1000 genomes]
rs7803475	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7805691	0.87[EUR][1000 genomes]
rs7805723	0.87[EUR][1000 genomes]
rs782902	0.85[EUR][1000 genomes]
rs919529	0.95[EUR][1000 genomes]
rs9642192	0.94[CEU][hapmap];0.89[EUR][1000 genomes]
rs9649677	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs993219	0.95[CEU][hapmap];0.89[EUR][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	nsv529344	chr7:83714286-84592857	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	nsv949446	chr7:84003501-84763823	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv34238	chr7:84279023-84591966	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv831050	chr7:84355996-84527261	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr7:84491400-84504400	Weak transcription	K562	blood

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