Variant report

Variant	rs7801001
Chromosome Location	chr7:40600069-40600070
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10226881	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs10228522	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10239229	1.00[AMR][1000 genomes]
rs10240076	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10241399	1.00[ASW][hapmap];0.91[LWK][hapmap];0.95[MKK][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes]
rs10260770	1.00[AMR][1000 genomes]
rs10262003	0.82[AFR][1000 genomes]
rs10264524	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10277710	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10282307	0.94[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1034804	1.00[ASW][hapmap];1.00[LWK][hapmap];0.95[MKK][hapmap];0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11486857	0.89[ASW][hapmap];1.00[AMR][1000 genomes]
rs17171725	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17171735	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17171746	0.94[YRI][hapmap];0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17171748	0.89[YRI][hapmap];0.85[AFR][1000 genomes]
rs17171754	0.89[ASW][hapmap];0.95[LWK][hapmap];0.91[MKK][hapmap];0.94[YRI][hapmap]
rs2214846	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28479858	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28565517	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28644197	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4492257	0.89[ASW][hapmap];0.95[LWK][hapmap];0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs57955744	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60699942	1.00[AMR][1000 genomes]
rs6943218	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6960628	0.83[YRI][hapmap]
rs6975971	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73310219	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7782395	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs7782411	0.94[YRI][hapmap];1.00[AMR][1000 genomes]
rs9886164	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030648	chr7:40218618-41032599	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1030515	chr7:40501867-40634808	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv887987	chr7:40505382-40748650	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv830971	chr7:40523075-40700172	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:40596000-40608400	Weak transcription	Aorta	Aorta
2	chr7:40599800-40604800	Weak transcription	Fetal Heart	heart

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