Variant report

Variant	rs16843745
Chromosome Location	chr2:141028684-141028685
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10166355	0.81[EUR][1000 genomes]
rs10803583	0.88[JPT][hapmap]
rs13018061	0.88[JPT][hapmap]
rs1388808	0.81[EUR][1000 genomes]
rs1471887	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1486969	0.81[EUR][1000 genomes]
rs1492389	0.86[ASN][1000 genomes]
rs1518439	0.89[JPT][hapmap]
rs1565638	0.81[EUR][1000 genomes]
rs16843663	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17470100	1.00[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17476635	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17477262	0.95[ASN][1000 genomes]
rs1829364	0.89[JPT][hapmap]
rs2129483	1.00[CEU][hapmap];0.88[JPT][hapmap];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs72892280	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72892291	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs901524	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834392	chr2:140920900-141086613	Flanking Active TSS Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv431757	chr2:140931289-141098020	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	esv2754266	chr2:141023643-141270786	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

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

what's new

Quick links