Variant report

Variant	rs6752912
Chromosome Location	chr2:145472933-145472934
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:145464586..145466817-chr2:145471212..145475328,4	K562	blood:

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs11674685	0.84[EUR][1000 genomes]
rs11675927	0.91[CEU][hapmap];0.84[EUR][1000 genomes]
rs11681525	0.84[EUR][1000 genomes]
rs11685274	0.84[EUR][1000 genomes]
rs11687464	0.84[EUR][1000 genomes]
rs11689322	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs11689575	0.91[CEU][hapmap];0.80[YRI][hapmap];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11691685	0.96[EUR][1000 genomes]
rs1559963	1.00[ASN][1000 genomes]
rs4384720	0.91[CEU][hapmap];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57477957	1.00[ASN][1000 genomes]
rs57834922	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58504774	1.00[ASN][1000 genomes]
rs58811157	1.00[ASN][1000 genomes]
rs59042570	1.00[ASN][1000 genomes]
rs66537831	0.94[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6718158	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6720379	1.00[ASN][1000 genomes]
rs67365209	0.84[EUR][1000 genomes]
rs67382063	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6756405	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67963154	0.96[EUR][1000 genomes]
rs68017203	0.94[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72850698	0.87[EUR][1000 genomes]
rs72852115	0.89[EUR][1000 genomes]
rs72852118	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72852120	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72852122	0.85[EUR][1000 genomes]
rs72852128	0.85[EUR][1000 genomes]
rs72852130	0.85[EUR][1000 genomes]
rs72852133	0.94[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72852135	0.85[EUR][1000 genomes]
rs72852137	0.85[EUR][1000 genomes]
rs72852150	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72852164	0.84[EUR][1000 genomes]
rs72852199	0.84[EUR][1000 genomes]
rs72853207	0.84[EUR][1000 genomes]
rs72853210	0.84[EUR][1000 genomes]
rs72853221	0.84[EUR][1000 genomes]
rs72853226	0.84[EUR][1000 genomes]
rs72853247	0.84[EUR][1000 genomes]
rs72853253	0.84[EUR][1000 genomes]
rs72853263	0.84[EUR][1000 genomes]
rs72993904	1.00[ASN][1000 genomes]
rs72993910	1.00[ASN][1000 genomes]
rs72997876	1.00[ASN][1000 genomes]
rs72999719	1.00[ASN][1000 genomes]
rs72999723	1.00[ASN][1000 genomes]
rs72999734	0.96[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72999737	1.00[ASN][1000 genomes]
rs72999751	1.00[ASN][1000 genomes]
rs72999753	1.00[ASN][1000 genomes]
rs73001719	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73001730	1.00[ASN][1000 genomes]
rs73001732	1.00[ASN][1000 genomes]
rs73001735	1.00[ASN][1000 genomes]
rs73001749	1.00[ASN][1000 genomes]
rs73001751	1.00[ASN][1000 genomes]
rs73001753	1.00[ASN][1000 genomes]
rs73001755	1.00[ASN][1000 genomes]
rs73001758	0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73003700	1.00[ASN][1000 genomes]
rs73005508	1.00[ASN][1000 genomes]
rs73005510	1.00[ASN][1000 genomes]
rs73962039	1.00[ASN][1000 genomes]
rs73962041	1.00[ASN][1000 genomes]
rs73963904	1.00[ASN][1000 genomes]
rs7595770	1.00[CEU][hapmap];0.87[EUR][1000 genomes];1.00[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	nsv1002563	chr2:145182201-145863253	Enhancers Weak transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv535957	chr2:145182201-145863253	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv529501	chr2:145257682-145485605	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv834397	chr2:145439528-145608628	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:145463200-145495600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr2:145464600-145473400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr2:145468600-145473400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr2:145470200-145473400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr2:145470200-145473600	Weak transcription	Aorta	Aorta

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