Variant report

Variant	rs4727596
Chromosome Location	chr7:104025663-104025664
allele	A/T
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:35)

rs_ID	r²[population]
rs10228106	0.90[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs10249235	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.88[YRI][hapmap]
rs10254627	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10487203	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10953427	0.83[YRI][hapmap]
rs10953428	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap]
rs10953432	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs1123760	0.90[CEU][hapmap]
rs12216592	0.84[YRI][hapmap]
rs12705208	0.85[CHB][hapmap]
rs1468143	0.95[CEU][hapmap];0.84[YRI][hapmap]
rs1468144	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap]
rs17390895	0.92[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap];0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1989823	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2040584	0.94[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs2188482	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.89[YRI][hapmap]
rs2188493	0.86[CHB][hapmap];0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs2188494	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap]
rs2214084	0.84[YRI][hapmap]
rs2214086	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap]
rs2214087	0.83[YRI][hapmap]
rs4236567	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4727599	0.95[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap]
rs4730001	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs4730002	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4730006	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap]
rs4730007	0.90[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap]
rs6465985	0.95[CEU][hapmap];1.00[CHB][hapmap];0.84[JPT][hapmap]
rs6946555	0.95[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6951873	0.95[CEU][hapmap];1.00[CHB][hapmap]
rs6952170	0.95[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap]
rs6959400	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap]
rs7778325	0.95[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];0.89[YRI][hapmap]
rs7790817	0.94[YRI][hapmap]
rs7798273	0.95[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.84[YRI][hapmap]

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	nsv608067	chr7:103944237-104029408	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No data

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