Variant report

Variant	rs17185435
Chromosome Location	chr4:91693756-91693757
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11735195	1.00[LWK][hapmap]
rs12507217	1.00[ASW][hapmap];0.90[CEU][hapmap];0.84[CHB][hapmap];0.80[MEX][hapmap];0.85[AFR][1000 genomes]
rs12509471	0.81[CEU][hapmap];0.82[GIH][hapmap]
rs1454329	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap]
rs1514743	0.80[CEU][hapmap]
rs17017522	0.81[CEU][hapmap];0.82[GIH][hapmap]
rs17183653	0.95[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap]
rs17183896	0.95[CEU][hapmap];0.95[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap];0.85[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap]
rs17185519	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17187179	0.90[CEU][hapmap];0.89[CHB][hapmap]
rs17188168	1.00[YRI][hapmap]
rs17243064	0.89[CEU][hapmap]
rs17243751	0.94[CEU][hapmap];0.94[CHB][hapmap];0.82[JPT][hapmap];0.84[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17244178	0.94[CEU][hapmap];0.83[GIH][hapmap];1.00[LWK][hapmap];0.94[MKK][hapmap];0.85[TSI][hapmap];0.86[EUR][1000 genomes]
rs17244283	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17245345	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17246676	0.90[CEU][hapmap];0.88[CHB][hapmap]
rs17247719	0.82[CHB][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs17248796	0.83[CEU][hapmap]
rs2904365	0.81[CEU][hapmap]
rs3796673	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs60127568	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6819756	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6833239	0.81[CEU][hapmap];0.82[GIH][hapmap]
rs6833272	1.00[ASW][hapmap];0.90[CEU][hapmap];0.89[CHB][hapmap];0.86[CHD][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs723781	0.85[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs723782	0.90[CEU][hapmap];0.85[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs749653	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7663098	0.95[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs7683055	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
2	nsv534470	chr4:91342219-91842807	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv428766	chr4:91618397-91768647	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv879552	chr4:91691313-91729462	Enhancers Active TSS Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases
5	nsv879553	chr4:91691313-91868576	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv879554	chr4:91692287-91731886	Enhancers Weak transcription Active TSS ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91692200-91696600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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