Variant report

Variant	rs1906951
Chromosome Location	chr3:159133359-159133360
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11917412	1.00[CEU][hapmap]
rs11917829	0.88[CEU][hapmap]
rs11917998	0.85[YRI][hapmap]
rs11920486	0.94[CEU][hapmap];0.86[EUR][1000 genomes]
rs12696092	1.00[CEU][hapmap]
rs13060178	0.81[CEU][hapmap]
rs13061579	1.00[CEU][hapmap]
rs13061619	1.00[CEU][hapmap]
rs13065679	1.00[CEU][hapmap]
rs13066122	0.94[CEU][hapmap]
rs13070853	0.93[CEU][hapmap]
rs13075790	1.00[CEU][hapmap]
rs13077258	1.00[CEU][hapmap]
rs13080892	0.94[CEU][hapmap]
rs13083244	1.00[CEU][hapmap]
rs13083887	0.93[CEU][hapmap]
rs13085008	1.00[CEU][hapmap]
rs13085667	1.00[CEU][hapmap]
rs13091349	0.83[CEU][hapmap]
rs13095658	0.93[CEU][hapmap]
rs1448996	1.00[CEU][hapmap]
rs1449002	0.94[CEU][hapmap]
rs1489913	1.00[YRI][hapmap]
rs17795417	1.00[CEU][hapmap]
rs1839219	1.00[CEU][hapmap]
rs2197852	0.85[YRI][hapmap]
rs2886480	1.00[CEU][hapmap]
rs34202807	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34566304	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35342196	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35556756	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35922036	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56264622	0.86[EUR][1000 genomes]
rs59583574	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61378344	0.86[EUR][1000 genomes]
rs61794665	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs61794673	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61795455	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6781001	0.83[CEU][hapmap]
rs6781285	0.94[CEU][hapmap]
rs6784143	1.00[CEU][hapmap]
rs7620377	1.00[CEU][hapmap]
rs7631740	0.94[CEU][hapmap]
rs7644770	1.00[CEU][hapmap]
rs870852	0.94[CEU][hapmap];0.85[EUR][1000 genomes]
rs9848338	1.00[CEU][hapmap]
rs9848831	1.00[CEU][hapmap]

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	nsv530059	chr3:158332590-159147549	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
2	nsv470971	chr3:158590928-159158217	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv998949	chr3:158774806-159394550	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1004990	chr3:159090974-159174954	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised 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

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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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