Variant report

Variant	rs992844
Chromosome Location	chr3:25111628-25111629
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11129178	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11715684	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12486699	0.81[AFR][1000 genomes]
rs12639346	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13060459	0.80[AMR][1000 genomes]
rs1609938	0.83[AFR][1000 genomes]
rs4858695	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4858699	0.81[AFR][1000 genomes]
rs6550941	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7626290	0.87[AFR][1000 genomes]
rs9811936	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9820537	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9823025	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs993803	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs993805	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[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	nsv834644	chr3:24936987-25112610	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv589955	chr3:24987823-25113358	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25104600-25112200	Weak transcription	Pancreas	Pancrea
2	chr3:25111200-25111800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr3:25111200-25112000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr3:25111400-25111800	Active TSS	Colon Smooth Muscle	Colon
5	chr3:25111400-25115600	Weak transcription	Fetal Lung	lung

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Input of quick search could be:

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

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