Variant report

Variant	rs73702918
Chromosome Location	chr8:111538737-111538738
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10505150	1.00[EUR][1000 genomes]
rs16880962	1.00[EUR][1000 genomes]
rs16880978	1.00[EUR][1000 genomes]
rs56144217	1.00[EUR][1000 genomes]
rs56409630	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61260614	1.00[EUR][1000 genomes]
rs73700909	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700910	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700911	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700913	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73700914	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702315	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702316	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702317	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702325	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702741	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702762	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702873	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73702874	1.00[EUR][1000 genomes]
rs73702875	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7828396	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024499	chr8:111190482-111691474	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv539717	chr8:111190482-111691474	ZNF genes & repeats Enhancers Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv611882	chr8:111342240-111722469	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1031119	chr8:111367939-111720763	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv891291	chr8:111462136-111681660	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv891292	chr8:111478321-111673039	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv2761460	chr8:111506457-111607147	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 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	chr8:111538400-111538800	Weak transcription	Placenta Amnion	Placenta Amnion

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