Variant report

Variant	rs13278793
Chromosome Location	chr8:69237570-69237571
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10098538	1.00[CEU][hapmap];0.98[TSI][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13251356	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13257807	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13261104	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13262740	0.96[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs13276394	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[TSI][hapmap]
rs1517124	0.90[CHB][hapmap];0.85[JPT][hapmap];0.83[ASN][1000 genomes]
rs1607144	0.89[CHB][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs1971404	0.96[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.87[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1971527	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2138677	0.92[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap];0.98[TSI][hapmap]
rs2176368	0.92[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs6472395	0.96[CEU][hapmap];0.98[TSI][hapmap]
rs6991818	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7000384	0.98[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7001418	0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7004646	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7013597	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7015549	0.90[CHB][hapmap];0.82[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7017437	0.88[CEU][hapmap];0.95[CHB][hapmap];0.90[JPT][hapmap]
rs7818147	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7822588	0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7823116	0.96[CEU][hapmap];0.91[CHB][hapmap];0.90[JPT][hapmap];0.95[TSI][hapmap];0.97[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7823422	0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7838935	0.85[CEU][hapmap];0.86[CHB][hapmap];0.83[EUR][1000 genomes]
rs814441	0.91[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs814444	0.91[CHB][hapmap];0.90[JPT][hapmap]
rs814446	0.81[JPT][hapmap]
rs814463	0.84[ASN][1000 genomes]
rs868546	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[TSI][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[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	nsv1028889	chr8:69026806-69308725	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv948687	chr8:69041121-69642540	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv890979	chr8:69176154-69252417	Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv890980	chr8:69181681-69252417	Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr8:69237400-69237600	Enhancers	Fetal Kidney	kidney
2	chr8:69237400-69237800	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr8:69237400-69238000	Enhancers	HUES48 Cell Line	embryonic stem cell

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