Variant report

Variant	rs7664025
Chromosome Location	chr4:91695919-91695920
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10025445	0.80[MKK][hapmap]
rs10856879	0.85[CHB][hapmap]
rs11097264	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs11722100	0.95[CHB][hapmap];0.93[JPT][hapmap];0.92[ASN][1000 genomes]
rs11726340	0.86[ASN][1000 genomes]
rs11730172	0.86[ASN][1000 genomes]
rs11730314	0.88[ASN][1000 genomes]
rs11731445	0.86[CHB][hapmap];0.87[JPT][hapmap];0.80[YRI][hapmap];0.85[ASN][1000 genomes]
rs11946210	0.86[CHB][hapmap]
rs12503213	0.86[CHB][hapmap]
rs12503263	0.86[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs13138129	0.85[ASW][hapmap];1.00[CHB][hapmap];0.82[LWK][hapmap]
rs1377916	0.86[CHB][hapmap];0.89[CHD][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs1399417	0.86[JPT][hapmap]
rs1399418	0.87[JPT][hapmap]
rs1454341	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs1514742	0.88[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];0.95[MKK][hapmap];0.95[TSI][hapmap];0.82[YRI][hapmap]
rs1598146	0.82[AFR][1000 genomes]
rs1598147	0.82[AFR][1000 genomes]
rs1606752	0.86[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs17184632	0.90[CHB][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs17185779	0.88[ASN][1000 genomes]
rs17186550	0.89[ASN][1000 genomes]
rs17245295	0.86[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs17245443	0.90[CHB][hapmap];0.91[CHD][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs17245485	0.87[ASN][1000 genomes]
rs17247544	0.86[CHB][hapmap]
rs1869539	0.86[YRI][hapmap]
rs2168075	0.83[ASN][1000 genomes]
rs2271592	0.83[ASN][1000 genomes]
rs2870264	0.86[ASN][1000 genomes]
rs3733451	0.87[JPT][hapmap]
rs4423844	0.86[ASN][1000 genomes]
rs4597790	0.85[ASN][1000 genomes]
rs59614972	0.87[ASN][1000 genomes]
rs62313023	0.93[ASN][1000 genomes]
rs62313024	0.88[ASN][1000 genomes]
rs6532239	0.95[CHB][hapmap];0.84[CHD][hapmap];0.93[JPT][hapmap];0.89[ASN][1000 genomes]
rs6532241	0.90[CHB][hapmap];0.89[CHD][hapmap];0.87[JPT][hapmap];0.88[ASN][1000 genomes]
rs6532242	0.86[ASN][1000 genomes]
rs6532243	0.91[ASN][1000 genomes]
rs6811504	0.92[ASN][1000 genomes]
rs6835028	0.90[CHB][hapmap];0.93[JPT][hapmap];0.87[ASN][1000 genomes]
rs7658990	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs7661466	0.86[ASN][1000 genomes]
rs7665447	0.90[CHB][hapmap];0.87[JPT][hapmap]
rs7670480	0.86[CHB][hapmap];0.87[JPT][hapmap];0.87[ASN][1000 genomes]
rs7683460	0.88[CHB][hapmap];0.84[JPT][hapmap]
rs7687983	0.87[ASN][1000 genomes]
rs7688114	0.87[JPT][hapmap]
rs897086	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs897088	0.86[ASN][1000 genomes]
rs976483	0.90[CHB][hapmap];0.83[CHD][hapmap];0.87[JPT][hapmap];0.87[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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