Variant report

Variant	rs73070728
Chromosome Location	chr1:194136892-194136893
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	chr1:194129570..194131258-chr1:194135186..194137115,2	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1487527	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16836190	1.00[AMR][1000 genomes]
rs16836491	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16836545	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16836597	1.00[AMR][1000 genomes]
rs56695737	1.00[AMR][1000 genomes]
rs60277362	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60574560	1.00[AMR][1000 genomes]
rs60860075	1.00[AMR][1000 genomes]
rs73052905	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73052916	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73052919	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73052931	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73052935	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73052944	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73053002	1.00[AMR][1000 genomes]
rs73055004	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73055015	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73056909	1.00[AMR][1000 genomes]
rs73056916	1.00[AMR][1000 genomes]
rs73056918	1.00[AMR][1000 genomes]
rs73056925	1.00[AMR][1000 genomes]
rs73056944	1.00[AMR][1000 genomes]
rs73064707	1.00[AMR][1000 genomes]
rs73064728	1.00[AMR][1000 genomes]
rs73070733	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070741	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070746	0.94[AFR][1000 genomes]
rs73070750	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070753	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070757	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73070766	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1008266	chr1:193550185-194481053	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv872834	chr1:193889533-194482304	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1001872	chr1:194030479-194288016	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv832181	chr1:194089117-194255615	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv872837	chr1:194106280-194221509	Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:194136600-194138000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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