Variant report

Variant	rs73842822
Chromosome Location	chr3:84792902-84792903
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs4470448	1.00[AMR][1000 genomes]
rs60728740	1.00[AMR][1000 genomes]
rs73842813	1.00[AMR][1000 genomes]
rs73842820	1.00[AMR][1000 genomes]
rs73842821	1.00[AMR][1000 genomes]
rs73842856	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845111	1.00[AMR][1000 genomes]
rs73845113	1.00[AMR][1000 genomes]
rs73845547	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3381298	chr3:84689266-85030314	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv877083	chr3:84720982-84819147	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1001316	chr3:84773522-85071342	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv877084	chr3:84779079-84819147	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	diseases
6	nsv460746	chr3:84779079-84833513	Enhancers Weak transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
7	nsv877085	chr3:84779079-84911212	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
8	nsv877086	chr3:84785709-84809350	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	n/a
9	nsv877087	chr3:84785709-84819147	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	n/a
10	nsv877088	chr3:84790582-84819147	Enhancers Weak transcription	lncRNA	n/a	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84791600-84793200	Enhancers	Fetal Brain Female	brain
2	chr3:84792000-84793200	Enhancers	Fetal Brain Male	brain
3	chr3:84792800-84793200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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

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