Variant report

Variant	rs6767494
Chromosome Location	chr3:158101447-158101448
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:158100498..158103302-chr3:158106866..158108793,2	K562	blood:

Extended variants
information (count: 76 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:69)

rs_ID	r²[population]
rs10936131	0.96[CEU][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10936132	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10936139	0.92[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10936143	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs10936145	0.89[JPT][hapmap]
rs11707386	0.92[CEU][hapmap];0.90[JPT][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11710813	0.82[JPT][hapmap]
rs11712563	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11715599	0.85[EUR][1000 genomes]
rs11716327	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs11716969	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11717618	0.92[CEU][hapmap];0.86[EUR][1000 genomes]
rs11717923	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs11719124	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11719153	0.90[CEU][hapmap];0.93[EUR][1000 genomes]
rs12053861	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12053865	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12053869	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12493128	0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12496934	0.92[CEU][hapmap];1.00[JPT][hapmap];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12631704	0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs12634807	1.00[CEU][hapmap];0.80[CHB][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12636733	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs12637649	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12639261	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12639310	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17627933	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17683939	0.92[CEU][hapmap];0.94[EUR][1000 genomes]
rs1851062	0.92[CEU][hapmap];0.91[EUR][1000 genomes]
rs1918000	0.93[EUR][1000 genomes]
rs2139696	0.91[EUR][1000 genomes]
rs34434866	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4402974	1.00[CEU][hapmap];1.00[JPT][hapmap]
rs4680421	0.92[CEU][hapmap];0.90[EUR][1000 genomes]
rs4680425	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4680428	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4680432	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4680435	0.92[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs56123505	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58195752	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58925169	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs60962704	0.90[EUR][1000 genomes]
rs6441193	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6772246	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6784968	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6800853	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6806967	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6807468	0.94[EUR][1000 genomes]
rs73164102	0.86[EUR][1000 genomes]
rs73166358	0.91[EUR][1000 genomes]
rs73168723	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs73168799	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73170303	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73170306	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73170310	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73170326	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73170331	0.81[EUR][1000 genomes]
rs73170337	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73170339	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73170346	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73170364	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs73170373	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73170375	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs73172105	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs73172114	0.82[ASN][1000 genomes]
rs73172119	0.86[ASN][1000 genomes]
rs7640075	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7641036	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7652970	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1013391	chr3:157505943-158115553	Flanking Active TSS Bivalent/Poised TSS Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv536775	chr3:157505943-158115553	Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1002378	chr3:157715428-158673414	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
4	nsv877689	chr3:157858930-158133307	Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv916910	chr3:157926799-158183372	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1014381	chr3:158070451-158350118	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1000904	chr3:158094357-158159317	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs6767494	RSRC1	Cis_1M	lymphoblastoid	RTeQTL
rs6767494	RP11-538P18.2	cis	lung	GTEx
rs6767494	RP11-538P18.2	cis	Skin Sun Exposed Lower leg	GTEx
rs6767494	RP11-538P18.2	cis	Nerve Tibial	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158100800-158113200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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