Variant report

Variant	rs13164446
Chromosome Location	chr5:116687802-116687803
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10036986	0.80[ASN][1000 genomes]
rs10039799	0.80[ASN][1000 genomes]
rs10039823	0.80[ASN][1000 genomes]
rs10069843	0.80[ASN][1000 genomes]
rs11749394	0.80[ASN][1000 genomes]
rs13159487	0.80[ASN][1000 genomes]
rs13172380	0.85[ASN][1000 genomes]
rs13187413	0.80[ASN][1000 genomes]
rs34173130	0.80[ASN][1000 genomes]
rs34205076	0.80[ASN][1000 genomes]
rs34227028	0.80[ASN][1000 genomes]
rs34411893	0.93[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs34937570	0.80[ASN][1000 genomes]
rs4259204	0.80[ASN][1000 genomes]
rs4443456	0.80[ASN][1000 genomes]
rs4448037	0.80[ASN][1000 genomes]
rs4457117	0.80[ASN][1000 genomes]
rs4458619	0.80[ASN][1000 genomes]
rs4464733	0.80[ASN][1000 genomes]
rs4464734	0.80[ASN][1000 genomes]
rs4469226	0.80[ASN][1000 genomes]
rs4552663	0.80[ASN][1000 genomes]
rs4568397	0.80[ASN][1000 genomes]
rs4593300	0.80[ASN][1000 genomes]
rs4629633	0.80[ASN][1000 genomes]
rs5011797	0.80[ASN][1000 genomes]
rs61332533	0.80[ASN][1000 genomes]
rs62380367	0.80[ASN][1000 genomes]
rs6595041	0.86[ASN][1000 genomes]
rs6860005	0.80[ASN][1000 genomes]
rs6869527	0.80[ASN][1000 genomes]
rs6870045	0.84[ASN][1000 genomes]
rs6870063	0.84[ASN][1000 genomes]
rs6879112	0.80[ASN][1000 genomes]
rs6888983	0.84[ASN][1000 genomes]
rs71593206	0.80[ASN][1000 genomes]
rs7447809	0.80[ASN][1000 genomes]
rs7712311	0.80[ASN][1000 genomes]
rs7712524	0.80[ASN][1000 genomes]
rs7715988	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7716581	0.85[ASN][1000 genomes]
rs7733520	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7733545	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv882755	chr5:116647725-116748877	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv16026	chr5:116682395-116693314	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv823188	chr5:116685962-116688101	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:116683600-116689000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr5:116687200-116697200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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