Variant report

Variant	rs73433823
Chromosome Location	chr7:120038414-120038415
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs57062655	1.00[AMR][1000 genomes]
rs57411631	1.00[AMR][1000 genomes]
rs57417999	1.00[AMR][1000 genomes]
rs57687096	1.00[AMR][1000 genomes]
rs58086739	1.00[AMR][1000 genomes]
rs58100103	1.00[AMR][1000 genomes]
rs58972047	1.00[AMR][1000 genomes]
rs59574653	1.00[AMR][1000 genomes]
rs60567357	1.00[AMR][1000 genomes]
rs60963172	1.00[AMR][1000 genomes]
rs61104791	1.00[AMR][1000 genomes]
rs61430585	1.00[AMR][1000 genomes]
rs61679179	1.00[AMR][1000 genomes]
rs73423706	1.00[AMR][1000 genomes]
rs73429960	1.00[AMR][1000 genomes]
rs73431913	1.00[AMR][1000 genomes]
rs73431916	1.00[AMR][1000 genomes]
rs73431930	1.00[AMR][1000 genomes]
rs73431937	1.00[AMR][1000 genomes]
rs73431947	1.00[AMR][1000 genomes]
rs73431954	1.00[AMR][1000 genomes]
rs73431966	1.00[AMR][1000 genomes]
rs73431968	1.00[AMR][1000 genomes]
rs73431971	1.00[AMR][1000 genomes]
rs73431979	1.00[AMR][1000 genomes]
rs73431984	1.00[AMR][1000 genomes]
rs73433807	1.00[AMR][1000 genomes]
rs73433825	1.00[AMR][1000 genomes]
rs73433829	1.00[AMR][1000 genomes]
rs73433838	1.00[AMR][1000 genomes]
rs73433844	1.00[AMR][1000 genomes]
rs73433850	1.00[AMR][1000 genomes]
rs73433858	1.00[AMR][1000 genomes]
rs73433862	1.00[AMR][1000 genomes]
rs73433873	1.00[AMR][1000 genomes]
rs73433887	1.00[AMR][1000 genomes]
rs73433890	1.00[AMR][1000 genomes]
rs73433898	1.00[AMR][1000 genomes]
rs73435825	1.00[AMR][1000 genomes]
rs73435842	1.00[AMR][1000 genomes]
rs73435846	1.00[AMR][1000 genomes]
rs73435868	1.00[AMR][1000 genomes]
rs73435875	1.00[AMR][1000 genomes]
rs73435881	1.00[AMR][1000 genomes]
rs73437806	1.00[AMR][1000 genomes]
rs73437842	1.00[AMR][1000 genomes]
rs73441827	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024920	chr7:120002420-120083753	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv516686	chr7:120015843-120223084	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv1026821	chr7:120020317-120190437	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120036400-120041800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:120038400-120039000	ZNF genes & repeats	GM12878-XiMat	blood

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