Variant report

Variant	rs1871738
Chromosome Location	chr4:128023339-128023340
allele	A/C
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:18)

rs_ID	r²[population]
rs10025761	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10033566	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12499978	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12503518	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12503648	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12507660	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12509041	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12649882	0.81[ASN][1000 genomes]
rs1471556	0.81[ASN][1000 genomes]
rs1480898	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1552089	1.00[CEU][hapmap];0.85[MEX][hapmap];0.93[TSI][hapmap];0.98[EUR][1000 genomes]
rs17212899	1.00[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17291185	0.93[EUR][1000 genomes]
rs17291532	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1871737	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2127818	0.81[ASN][1000 genomes]
rs4385081	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7659822	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv879914	chr4:128005362-128123638	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128019000-128024200	Weak transcription	Fetal Brain Male	brain
2	chr4:128023200-128025800	Enhancers	Fetal Lung	lung

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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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