Variant report

Variant	rs13098545
Chromosome Location	chr3:60752914-60752915
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:60605481..60608081-chr3:60751441..60753004,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11130781	0.87[ASN][1000 genomes]
rs11130782	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11710207	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12185984	0.89[ASN][1000 genomes]
rs13059280	0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13065371	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13067083	0.99[ASN][1000 genomes]
rs13098348	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13098466	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13099811	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1569346	0.87[ASN][1000 genomes]
rs2064012	0.81[ASN][1000 genomes]
rs2142294	0.85[ASN][1000 genomes]
rs2205342	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2205343	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2205344	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2364293	0.82[ASN][1000 genomes]
rs2594170	0.82[ASN][1000 genomes]
rs2594171	0.82[ASN][1000 genomes]
rs2736731	0.82[ASN][1000 genomes]
rs4974227	0.97[ASN][1000 genomes]
rs57203484	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57595293	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6762120	0.82[ASN][1000 genomes]
rs6762122	0.81[ASN][1000 genomes]
rs6764320	0.82[ASN][1000 genomes]
rs6771383	0.87[ASN][1000 genomes]
rs6786213	0.92[ASN][1000 genomes]
rs6787897	0.89[ASN][1000 genomes]
rs7429680	0.98[ASN][1000 genomes]
rs926139	0.83[ASN][1000 genomes]
rs9754707	0.82[ASN][1000 genomes]
rs9840977	0.98[ASN][1000 genomes]
rs9842407	0.89[ASN][1000 genomes]
rs9847131	0.89[ASN][1000 genomes]
rs9881274	0.99[ASN][1000 genomes]
rs9882068	1.00[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	nsv529602	chr3:60088353-60830769	Enhancers Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv998815	chr3:60495872-60830769	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv999828	chr3:60537384-60785274	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:60746200-60756200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:60747200-60756000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr3:60747200-60756400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:60752000-60754200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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