Variant report

Variant	rs8013610
Chromosome Location	chr14:81083771-81083772
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11159470	0.82[ASN][1000 genomes]
rs12589109	0.82[ASN][1000 genomes]
rs17519	0.87[ASN][1000 genomes]
rs34201956	0.86[ASN][1000 genomes]
rs4903927	0.84[ASN][1000 genomes]
rs4903930	0.82[ASN][1000 genomes]
rs6574592	0.87[ASN][1000 genomes]
rs66523962	0.83[ASN][1000 genomes]
rs7142417	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7152126	0.84[ASN][1000 genomes]
rs7158869	0.82[ASN][1000 genomes]
rs7159302	0.82[ASN][1000 genomes]
rs8003492	0.87[ASN][1000 genomes]
rs8013202	0.82[ASN][1000 genomes]
rs8018031	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr14:81076200-81086600	Weak transcription	A549	lung
2	chr14:81083400-81109400	Weak transcription	Dnd41	blood
3	chr14:81083600-81088200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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