Variant report

Variant	rs73433797
Chromosome Location	chr7:122233623-122233624
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:122233367..122235996-chr7:122236414..122239821,3	K562	blood:

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs11767048	0.94[ASN][1000 genomes]
rs59716073	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73433732	0.90[AFR][1000 genomes]
rs73433735	0.90[AFR][1000 genomes]
rs73433740	0.90[AFR][1000 genomes]
rs73433744	0.90[AFR][1000 genomes]
rs73433750	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433754	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433759	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433764	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433769	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433771	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433772	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs73433778	0.90[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs73433780	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73433782	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73433784	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73433787	0.90[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73433793	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73433800	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73433802	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435706	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435725	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73435731	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9918663	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017029	chr7:121958574-122338623	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv532178	chr7:122203056-122978846	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 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	chr7:122217600-122265600	Weak transcription	Aorta	Aorta
2	chr7:122231200-122246200	Weak transcription	Left Ventricle	heart

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