Variant report

Variant	rs9576685
Chromosome Location	chr13:39570893-39570894
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 79 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs11147745	0.99[ASN][1000 genomes]
rs12428445	0.99[ASN][1000 genomes]
rs12429324	0.99[ASN][1000 genomes]
rs12429338	0.99[ASN][1000 genomes]
rs12430450	0.99[ASN][1000 genomes]
rs12431316	1.00[ASN][1000 genomes]
rs1326405	0.95[ASN][1000 genomes]
rs17058947	0.99[ASN][1000 genomes]
rs17058990	0.95[ASN][1000 genomes]
rs17059014	0.95[ASN][1000 genomes]
rs2094252	1.00[ASN][1000 genomes]
rs2094253	1.00[ASN][1000 genomes]
rs2094254	1.00[ASN][1000 genomes]
rs2104518	1.00[ASN][1000 genomes]
rs2274384	0.91[ASN][1000 genomes]
rs2274385	0.99[ASN][1000 genomes]
rs2296648	0.99[ASN][1000 genomes]
rs34316151	1.00[ASN][1000 genomes]
rs34327528	1.00[ASN][1000 genomes]
rs35804724	0.95[ASN][1000 genomes]
rs35864330	1.00[ASN][1000 genomes]
rs3751377	0.99[ASN][1000 genomes]
rs3751378	0.99[ASN][1000 genomes]
rs3751379	0.99[ASN][1000 genomes]
rs3812879	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4142398	0.85[ASN][1000 genomes]
rs55809136	0.95[ASN][1000 genomes]
rs66496062	1.00[ASN][1000 genomes]
rs66908302	0.99[ASN][1000 genomes]
rs67296293	0.99[ASN][1000 genomes]
rs73169457	1.00[ASN][1000 genomes]
rs7317852	0.95[ASN][1000 genomes]
rs7318688	0.95[ASN][1000 genomes]
rs7327748	0.95[ASN][1000 genomes]
rs747752	0.99[ASN][1000 genomes]
rs7987207	0.99[ASN][1000 genomes]
rs7994530	0.87[ASN][1000 genomes]
rs7997052	0.98[ASN][1000 genomes]
rs7998475	1.00[ASN][1000 genomes]
rs8000929	0.95[ASN][1000 genomes]
rs9566385	0.88[ASN][1000 genomes]
rs9566389	0.99[ASN][1000 genomes]
rs9566391	0.95[ASN][1000 genomes]
rs9566393	0.95[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9566396	0.85[ASN][1000 genomes]
rs9566397	0.86[AMR][1000 genomes]
rs9576669	0.87[ASN][1000 genomes]
rs9576670	0.99[ASN][1000 genomes]
rs9576673	0.97[ASN][1000 genomes]
rs9576674	0.99[ASN][1000 genomes]
rs9576676	0.99[ASN][1000 genomes]
rs9576677	0.99[ASN][1000 genomes]
rs9576678	0.99[ASN][1000 genomes]
rs9576679	0.97[ASN][1000 genomes]
rs9576681	1.00[ASN][1000 genomes]
rs9576683	1.00[ASN][1000 genomes]
rs9576684	1.00[ASN][1000 genomes]
rs9576686	1.00[ASN][1000 genomes]
rs9576688	1.00[ASN][1000 genomes]
rs9576690	0.99[ASN][1000 genomes]
rs9576691	0.83[ASN][1000 genomes]
rs9576692	1.00[ASN][1000 genomes]
rs9576693	0.98[ASN][1000 genomes]
rs9576695	1.00[ASN][1000 genomes]
rs9576696	0.99[ASN][1000 genomes]
rs9576697	0.99[ASN][1000 genomes]
rs9576698	0.99[ASN][1000 genomes]
rs9576699	0.99[ASN][1000 genomes]
rs9576700	0.99[ASN][1000 genomes]
rs9576701	0.95[ASN][1000 genomes]
rs9576703	0.93[ASN][1000 genomes]
rs9576705	0.95[ASN][1000 genomes]
rs9576707	0.95[ASN][1000 genomes]
rs9576710	0.87[ASN][1000 genomes]
rs9576711	0.87[ASN][1000 genomes]
rs9576717	0.85[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	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	esv2753642	chr13:39522300-39649000	Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
3	esv2753553	chr13:39526600-39649000	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39568000-39571800	Weak transcription	K562	blood
2	chr13:39570800-39571600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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