Variant report

Variant	rs7673595
Chromosome Location	chr4:110269265-110269266
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10005198	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10007410	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10155246	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11933172	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11939924	0.84[EUR][1000 genomes]
rs12641197	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12641272	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13104799	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13113384	0.87[EUR][1000 genomes]
rs13119700	0.87[EUR][1000 genomes]
rs13126829	0.83[EUR][1000 genomes]
rs13138833	0.87[EUR][1000 genomes]
rs1557804	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17842269	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1859144	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1859146	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1859147	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1981540	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1981541	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2079108	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2214377	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2346014	0.87[EUR][1000 genomes]
rs28374470	0.88[EUR][1000 genomes]
rs28463999	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28542804	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28585579	0.87[EUR][1000 genomes]
rs28628718	0.87[EUR][1000 genomes]
rs28749845	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4524460	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6533426	0.87[EUR][1000 genomes]
rs6825928	1.00[CEU][hapmap]
rs6827985	0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6841133	0.87[EUR][1000 genomes]
rs6841222	0.87[EUR][1000 genomes]
rs7665024	0.83[EUR][1000 genomes]
rs7673867	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7675344	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7680752	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7680920	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7684744	0.87[EUR][1000 genomes]
rs7685787	0.87[EUR][1000 genomes]
rs7694523	0.83[EUR][1000 genomes]
rs7695754	1.00[CEU][hapmap]
rs7699247	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs876464	0.87[EUR][1000 genomes]
rs9307329	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9993228	0.87[EUR][1000 genomes]
rs9996165	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9996432	0.87[EUR][1000 genomes]
rs9996537	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9996920	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9999270	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9999278	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9999751	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 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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