Variant report

Variant	rs1383520
Chromosome Location	chr4:128039143-128039144
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1000707	0.85[EUR][1000 genomes]
rs10012435	0.85[EUR][1000 genomes]
rs10518518	0.85[EUR][1000 genomes]
rs11098914	0.85[EUR][1000 genomes]
rs11098915	0.85[EUR][1000 genomes]
rs11098916	0.85[EUR][1000 genomes]
rs11098917	0.85[EUR][1000 genomes]
rs13116630	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1351425	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1351426	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1480897	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1480909	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1480910	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17213081	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17228715	0.85[EUR][1000 genomes]
rs17228756	0.85[EUR][1000 genomes]
rs17228875	0.85[EUR][1000 genomes]
rs17229246	0.85[EUR][1000 genomes]
rs17229576	0.83[EUR][1000 genomes]
rs17278402	0.94[ASN][1000 genomes]
rs17291337	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17293310	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17293345	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs17293359	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17294432	0.85[EUR][1000 genomes]
rs17294586	0.85[EUR][1000 genomes]
rs17294663	0.85[EUR][1000 genomes]
rs17295431	0.82[EUR][1000 genomes]
rs28524825	0.85[EUR][1000 genomes]
rs34120215	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4550943	0.85[EUR][1000 genomes]
rs4550946	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs55773382	0.84[EUR][1000 genomes]
rs55824976	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56216620	0.85[EUR][1000 genomes]
rs56387802	0.85[EUR][1000 genomes]
rs62333871	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs62333879	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62333900	0.84[EUR][1000 genomes]
rs62333901	0.85[EUR][1000 genomes]
rs62333902	0.85[EUR][1000 genomes]
rs62333903	0.85[EUR][1000 genomes]
rs62333904	0.85[EUR][1000 genomes]
rs62333905	0.85[EUR][1000 genomes]
rs62333906	0.85[EUR][1000 genomes]
rs62333907	0.85[EUR][1000 genomes]
rs62333908	0.85[EUR][1000 genomes]
rs62335164	0.83[EUR][1000 genomes]
rs62335485	0.96[ASN][1000 genomes]
rs62335489	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62335523	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs62335528	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6810678	0.85[EUR][1000 genomes]
rs6836252	0.82[EUR][1000 genomes]
rs6836483	0.85[EUR][1000 genomes]
rs6853523	0.85[EUR][1000 genomes]
rs6857872	0.84[EUR][1000 genomes]
rs6857937	0.85[EUR][1000 genomes]
rs6858838	0.85[EUR][1000 genomes]
rs72680008	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72680022	0.85[EUR][1000 genomes]
rs7655646	0.81[EUR][1000 genomes]
rs7694318	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs976814	0.96[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs998857	0.85[EUR][1000 genomes]
rs998858	0.85[EUR][1000 genomes]
rs999285	0.85[EUR][1000 genomes]

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	nsv879914	chr4:128005362-128123638	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128038600-128042000	Weak transcription	Fetal Brain Male	brain

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