Variant report

Variant	rs73435806
Chromosome Location	chr7:120081939-120081940
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs58182881	0.82[AFR][1000 genomes]
rs60202137	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73429988	0.82[AFR][1000 genomes]
rs73429998	0.82[AFR][1000 genomes]
rs73431924	0.82[AFR][1000 genomes]
rs73431934	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431939	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431940	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431941	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431945	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431949	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431961	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431967	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431976	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431981	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431995	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73431997	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433810	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433856	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433871	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73433896	0.90[AFR][1000 genomes]
rs73435860	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73435864	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73435871	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73435874	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73435889	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73435902	0.85[AFR][1000 genomes]
rs73437811	0.85[AFR][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	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
4	nsv970423	chr7:120081849-120085097	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120081600-120083000	Flanking Active TSS	GM12878-XiMat	blood

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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