Variant report

Variant	rs978137
Chromosome Location	chr8:54484442-54484443
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:54482970..54485884-chr8:54754833..54757181,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000047249	Chromatin interaction

Extended variants
information (count: 131 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:128)

rs_ID	r²[population]
rs10112441	0.86[ASN][1000 genomes]
rs10808882	1.00[ASN][1000 genomes]
rs10958375	0.91[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10958376	1.00[ASN][1000 genomes]
rs10958377	0.92[ASN][1000 genomes]
rs10958378	0.92[ASN][1000 genomes]
rs10958379	0.86[ASN][1000 genomes]
rs10958380	0.86[ASN][1000 genomes]
rs10958386	0.86[ASN][1000 genomes]
rs11778297	0.81[ASN][1000 genomes]
rs11779176	0.86[ASN][1000 genomes]
rs11779309	0.94[ASN][1000 genomes]
rs11779641	1.00[ASN][1000 genomes]
rs11785377	1.00[ASN][1000 genomes]
rs11785465	0.86[ASN][1000 genomes]
rs11785489	0.86[ASN][1000 genomes]
rs11987300	0.86[ASN][1000 genomes]
rs11995715	0.86[ASN][1000 genomes]
rs12547226	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12549885	0.86[ASN][1000 genomes]
rs12549903	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12549929	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12550388	0.86[ASN][1000 genomes]
rs13249182	0.86[ASN][1000 genomes]
rs13249232	0.86[ASN][1000 genomes]
rs13251373	0.86[ASN][1000 genomes]
rs13253006	0.86[ASN][1000 genomes]
rs13259310	1.00[ASN][1000 genomes]
rs13260243	0.86[ASN][1000 genomes]
rs13266723	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13268670	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13274248	0.86[ASN][1000 genomes]
rs13275215	0.86[ASN][1000 genomes]
rs1382123	1.00[ASN][1000 genomes]
rs1382125	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1477960	1.00[ASN][1000 genomes]
rs1477964	0.97[ASN][1000 genomes]
rs1477965	0.97[ASN][1000 genomes]
rs1477966	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1551910	1.00[ASN][1000 genomes]
rs1551911	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1551913	1.00[ASN][1000 genomes]
rs2035197	1.00[ASN][1000 genomes]
rs2086071	1.00[ASN][1000 genomes]
rs2086072	0.81[ASN][1000 genomes]
rs2086073	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2086074	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2086075	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2169693	1.00[ASN][1000 genomes]
rs2199590	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2199591	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28521998	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs3919868	1.00[ASN][1000 genomes]
rs3940882	1.00[ASN][1000 genomes]
rs4258030	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4531078	0.94[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4873261	1.00[ASN][1000 genomes]
rs4873759	1.00[ASN][1000 genomes]
rs6415668	1.00[ASN][1000 genomes]
rs6415669	0.86[ASN][1000 genomes]
rs6415672	0.86[ASN][1000 genomes]
rs6415673	0.86[ASN][1000 genomes]
rs6415675	0.86[ASN][1000 genomes]
rs6473856	0.92[ASN][1000 genomes]
rs6473860	0.86[ASN][1000 genomes]
rs6473861	0.86[ASN][1000 genomes]
rs6473862	0.86[ASN][1000 genomes]
rs6473863	0.86[ASN][1000 genomes]
rs6473864	0.86[ASN][1000 genomes]
rs6473865	0.86[ASN][1000 genomes]
rs6473866	0.86[ASN][1000 genomes]
rs6473867	0.86[ASN][1000 genomes]
rs6473868	0.86[ASN][1000 genomes]
rs6473869	0.86[ASN][1000 genomes]
rs6473871	0.86[ASN][1000 genomes]
rs6473872	0.86[ASN][1000 genomes]
rs6473875	0.82[ASN][1000 genomes]
rs6473876	0.86[ASN][1000 genomes]
rs66931312	0.82[ASN][1000 genomes]
rs6983383	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6989219	0.86[ASN][1000 genomes]
rs6989676	0.86[ASN][1000 genomes]
rs6990694	0.86[ASN][1000 genomes]
rs6991676	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6991825	1.00[ASN][1000 genomes]
rs6996204	1.00[ASN][1000 genomes]
rs7008144	0.86[ASN][1000 genomes]
rs7009049	0.86[ASN][1000 genomes]
rs7010314	0.86[ASN][1000 genomes]
rs7386224	0.86[ASN][1000 genomes]
rs7387992	0.86[ASN][1000 genomes]
rs7388189	0.86[ASN][1000 genomes]
rs7388300	0.86[ASN][1000 genomes]
rs7388337	0.86[ASN][1000 genomes]
rs7459503	0.86[ASN][1000 genomes]
rs7459559	0.86[ASN][1000 genomes]
rs7459598	0.86[ASN][1000 genomes]
rs7460037	0.86[ASN][1000 genomes]
rs7460923	0.86[ASN][1000 genomes]
rs7460945	0.86[ASN][1000 genomes]
rs7461003	0.82[ASN][1000 genomes]
rs7461174	0.86[ASN][1000 genomes]
rs7461405	0.92[ASN][1000 genomes]
rs7461954	1.00[ASN][1000 genomes]
rs7462195	0.86[ASN][1000 genomes]
rs7462220	0.82[ASN][1000 genomes]
rs7462612	0.86[ASN][1000 genomes]
rs7462827	0.86[ASN][1000 genomes]
rs7462881	0.86[ASN][1000 genomes]
rs7462940	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7463378	0.86[ASN][1000 genomes]
rs7463478	0.86[ASN][1000 genomes]
rs7463519	0.86[ASN][1000 genomes]
rs7464824	0.86[ASN][1000 genomes]
rs7465481	0.86[ASN][1000 genomes]
rs7465505	0.86[ASN][1000 genomes]
rs7465593	0.86[ASN][1000 genomes]
rs7465617	0.86[ASN][1000 genomes]
rs7465670	0.86[ASN][1000 genomes]
rs7820396	0.86[ASN][1000 genomes]
rs7825736	1.00[ASN][1000 genomes]
rs7842388	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9643813	0.86[ASN][1000 genomes]
rs9643814	0.86[ASN][1000 genomes]
rs978138	1.00[ASN][1000 genomes]
rs978139	0.97[ASN][1000 genomes]
rs978140	1.00[ASN][1000 genomes]
rs979361	0.97[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	esv1813750	chr8:54471135-54528984	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2758159	chr8:54474589-54737473	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	esv2759616	chr8:54474589-54737473	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS 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:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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