Variant report

Variant	rs1507787
Chromosome Location	chr4:131016112-131016113
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11099034	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11099037	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11933622	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11933661	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12501049	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12501100	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12502233	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12505406	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12508682	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13114373	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13115242	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13122937	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13127316	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13134721	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13150131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13150371	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13152596	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1395977	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1395978	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4863960	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4864333	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4864335	0.82[EUR][1000 genomes]
rs4864336	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4864351	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4864352	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4864353	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6844823	0.87[ASN][1000 genomes]
rs7668591	0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9985771	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv595414	chr4:130983055-131024471	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
2	nsv595415	chr4:130983605-131046911	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv595416	chr4:130998472-131834405	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv2762461	chr4:131004382-131391658	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr4:131014600-131020000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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