Variant report

Variant	rs59707679
Chromosome Location	chr6:70685340-70685341
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:70683823..70685555-chr6:70687830..70690193,2	K562	blood:
2	chr6:70680703..70682726-chr6:70685209..70687558,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10485244	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12110870	0.85[EUR][1000 genomes]
rs17766479	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2096058	0.88[ASN][1000 genomes]
rs2345744	0.82[EUR][1000 genomes]
rs3793031	0.87[EUR][1000 genomes]
rs3793032	0.85[EUR][1000 genomes]
rs3793033	0.87[EUR][1000 genomes]
rs3793035	0.85[EUR][1000 genomes]
rs3793036	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805961	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805962	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805966	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805968	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805971	0.89[AMR][1000 genomes]
rs3805973	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3805977	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56293172	0.87[EUR][1000 genomes]
rs56922945	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs58134065	0.85[EUR][1000 genomes]
rs59501442	0.87[EUR][1000 genomes]
rs59599861	0.87[EUR][1000 genomes]
rs60134810	0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6903421	0.87[EUR][1000 genomes]
rs6938320	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7742627	0.87[EUR][1000 genomes]
rs7761968	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446169	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9446170	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9446172	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9446178	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9454908	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9454910	0.82[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs9454914	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9454937	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886140	chr6:70354682-70728202	Strong transcription Enhancers Genic enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv886141	chr6:70590638-70694162	Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1026151	chr6:70621616-70946967	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv463151	chr6:70625166-70694162	Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv603636	chr6:70625166-70694162	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv470832	chr6:70654657-70767756	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv603637	chr6:70658432-70740151	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv603638	chr6:70658432-70740306	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv933674	chr6:70663616-70973112	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
10	esv2755013	chr6:70672128-70694162	Strong transcription Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:70672400-70697600	Weak transcription	GM12878-XiMat	blood
2	chr6:70682800-70686600	Strong transcription	Primary B cells from cord blood	blood
3	chr6:70683000-70685400	Enhancers	Fetal Heart	heart
4	chr6:70683800-70686400	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:70684000-70686800	Strong transcription	Primary B cells from peripheral blood	blood

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