Variant report

Variant	rs6943555
Chromosome Location	chr7:69806023-69806024
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 84 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10229027	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10229155	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10234614	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10234844	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10234892	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10237530	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10237685	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10244275	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10246631	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10251306	0.87[ASN][1000 genomes]
rs10251416	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10254839	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10256062	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10256186	0.88[ASN][1000 genomes]
rs10258298	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10258962	0.90[EUR][1000 genomes]
rs10270616	0.80[ASN][1000 genomes]
rs10277411	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10279392	0.80[ASN][1000 genomes]
rs10280622	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10486874	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10486875	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10499812	0.88[ASN][1000 genomes]
rs10950199	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11766329	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12112638	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12155138	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12374873	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12698849	0.80[ASN][1000 genomes]
rs12698866	0.88[ASN][1000 genomes]
rs12698877	0.91[ASN][1000 genomes]
rs12698895	1.00[CEU][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12698896	1.00[CEU][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12698897	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12698899	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13221252	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13226923	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1357759	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1404274	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1464786	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1464787	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1464788	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs1524518	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1880368	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2103132	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2222544	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2280613	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2280614	0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2866277	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35303761	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs3846984	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6460541	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6460542	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6460543	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6953344	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6954715	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6954837	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6957740	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6967697	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6967986	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6969375	0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6976581	0.91[EUR][1000 genomes]
rs7781035	0.92[ASN][1000 genomes]
rs7781401	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7781727	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7787612	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7788024	0.92[ASN][1000 genomes]
rs7790934	0.92[ASN][1000 genomes]
rs7792775	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7792964	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7798991	0.90[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7799308	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7808540	0.92[ASN][1000 genomes]
rs8180850	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9638268	0.83[ASN][1000 genomes]
rs9918496	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9918544	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[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	nsv1018749	chr7:69149029-69995112	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv532782	chr7:69383651-70189959	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv869342	chr7:69671501-69958576	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv607431	chr7:69699074-69828729	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv888337	chr7:69707076-69952187	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv529669	chr7:69709373-69974708	Enhancers Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1028870	chr7:69742438-69879231	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Alcohol consumption	21471458	GWAS catalog

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69800600-69806600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr7:69803000-69819600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr7:69804200-69807600	Enhancers	Fetal Brain Female	brain
4	chr7:69805600-69806400	Weak transcription	Fetal Brain Male	brain
5	chr7:69806000-69806200	Bivalent Enhancer	Brain Germinal Matrix	brain
6	chr7:69806000-69806200	Enhancers	Fetal Lung	lung

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