Variant report

Variant	rs6940864
Chromosome Location	chr6:77949759-77949760
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10943431	0.82[EUR][1000 genomes]
rs11753132	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11756056	0.98[AFR][1000 genomes]
rs11758490	0.98[AFR][1000 genomes]
rs11965009	0.82[AMR][1000 genomes]
rs13190810	0.83[EUR][1000 genomes]
rs13190872	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs13194850	0.98[AFR][1000 genomes]
rs13200434	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13200769	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13215989	0.85[EUR][1000 genomes]
rs13220732	0.83[EUR][1000 genomes]
rs13220843	0.83[EUR][1000 genomes]
rs2000223	0.84[EUR][1000 genomes]
rs2153887	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2153888	0.82[EUR][1000 genomes]
rs28860022	0.82[EUR][1000 genomes]
rs4329077	0.82[EUR][1000 genomes]
rs4469255	0.82[EUR][1000 genomes]
rs4547978	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4551143	0.82[EUR][1000 genomes]
rs6899503	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6906746	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6907507	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6912240	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6913130	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6914286	0.83[EUR][1000 genomes]
rs6919231	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6920021	0.98[AFR][1000 genomes]
rs6934081	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6934297	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6934501	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6934611	0.83[EUR][1000 genomes]
rs6934854	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6939523	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6939863	0.98[AFR][1000 genomes]
rs6940394	0.98[AFR][1000 genomes]
rs7745859	0.94[AFR][1000 genomes]
rs7746318	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7750699	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7750813	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7768260	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7768511	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9294068	0.82[EUR][1000 genomes]
rs9294069	0.82[EUR][1000 genomes]
rs9443366	0.98[AFR][1000 genomes]
rs9443370	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9443371	0.84[EUR][1000 genomes]
rs9443372	0.84[EUR][1000 genomes]
rs9443374	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9443375	0.83[EUR][1000 genomes]
rs9443377	0.82[EUR][1000 genomes]
rs9443379	0.85[AMR][1000 genomes]
rs9443380	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9448006	0.98[AFR][1000 genomes]
rs9448007	0.98[AFR][1000 genomes]
rs9448009	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9448013	0.84[EUR][1000 genomes]
rs9448014	0.84[EUR][1000 genomes]
rs9448018	0.84[EUR][1000 genomes]
rs9448020	0.82[EUR][1000 genomes]
rs9448026	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9448032	0.82[EUR][1000 genomes]
rs9448042	0.83[EUR][1000 genomes]
rs9448043	0.82[EUR][1000 genomes]
rs9448044	0.82[EUR][1000 genomes]
rs9448045	0.82[EUR][1000 genomes]
rs9448046	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9448047	0.89[AMR][1000 genomes];0.96[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	nsv1017082	chr6:77585310-78258237	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv3417770	chr6:77670473-77963253	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3402238	chr6:77670497-77963278	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv886223	chr6:77686247-77950949	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv534282	chr6:77764575-78351994	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1034979	chr6:77781244-78426249	Active TSS Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv538324	chr6:77781244-78426249	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv2753543	chr6:77791848-78059351	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1015307	chr6:77902559-78352291	Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	esv1795494	chr6:77933591-77953420	Enhancers Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:77933200-77957000	Weak transcription	Aorta	Aorta
2	chr6:77941800-77952600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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