Variant report

Variant	rs746596
Chromosome Location	chr8:110984472-110984473
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10098219	1.00[CEU][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16880206	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16880222	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs16880283	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs16880295	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1948891	1.00[GIH][hapmap]
rs2218815	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28719776	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28720015	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6997471	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7003810	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7012869	1.00[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs735913	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.85[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7822930	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7831509	0.89[EUR][1000 genomes]
rs7833678	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.82[EUR][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	nsv1033321	chr8:110826297-111131801	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1019284	chr8:110866196-111221890	Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv831421	chr8:110874634-111038295	Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv6347	chr8:110978143-111023190	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:110977800-110986000	Weak transcription	Spleen	Spleen
2	chr8:110983600-110986000	Active TSS	Brain Inferior Temporal Lobe	brain
3	chr8:110983600-110986800	Active TSS	Fetal Brain Female	brain
4	chr8:110984000-110986000	Weak transcription	Colonic Mucosa	Colon
5	chr8:110984200-110985800	Active TSS	Brain Angular Gyrus	brain
6	chr8:110984400-110984600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:110984400-110984800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr8:110984400-110985000	Enhancers	Fetal Brain Male	brain
9	chr8:110984400-110985000	Strong transcription	Rectal Mucosa Donor 29	rectum

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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