Variant report

Variant	rs13113216
Chromosome Location	chr4:80165840-80165841
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:80130888..80132552-chr4:80164222..80166860,2	K562	blood:
2	chr4:80130065..80132388-chr4:80165360..80168173,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10015645	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10518214	1.00[ASN][1000 genomes]
rs1471729	1.00[ASN][1000 genomes]
rs17003679	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28455975	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28460261	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28546466	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28651876	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28656884	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28688839	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28704600	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28727508	1.00[ASN][1000 genomes]
rs34078327	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34655076	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4246716	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4246717	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4308381	0.84[EUR][1000 genomes]
rs4413431	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59072456	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6816121	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6821709	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6853888	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6858130	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72662701	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664018	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73828224	1.00[ASN][1000 genomes]
rs73828232	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7681755	1.00[ASN][1000 genomes]
rs9790513	1.00[ASN][1000 genomes]
rs982992	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9991698	0.84[EUR][1000 genomes];1.00[ASN][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	nsv1000907	chr4:79838948-80224764	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv879505	chr4:79887043-80293046	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:80159800-80166400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:80165400-80171200	Weak transcription	K562	blood
3	chr4:80165400-80194000	Weak transcription	Aorta	Aorta

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