Variant report

Variant	rs4372844
Chromosome Location	chr2:189108883-189108884
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 57 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10221554	0.98[ASN][1000 genomes]
rs10931341	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11676580	0.94[ASN][1000 genomes]
rs12151472	0.81[JPT][hapmap]
rs12151502	0.84[JPT][hapmap]
rs12614592	0.95[ASN][1000 genomes]
rs13389609	0.98[ASN][1000 genomes]
rs13403138	0.98[ASN][1000 genomes]
rs13416775	1.00[CHB][hapmap];0.88[JPT][hapmap];0.98[ASN][1000 genomes]
rs13432874	0.98[ASN][1000 genomes]
rs16829913	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16829916	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16829926	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs34477786	0.98[ASN][1000 genomes]
rs4337443	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4371324	0.98[ASN][1000 genomes]
rs4453654	0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs4490147	1.00[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4536617	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4541223	0.98[ASN][1000 genomes]
rs4552156	0.94[ASN][1000 genomes]
rs4595930	0.98[ASN][1000 genomes]
rs60688387	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs66579041	0.98[ASN][1000 genomes]
rs66725342	0.98[ASN][1000 genomes]
rs6707721	0.98[ASN][1000 genomes]
rs6708455	0.94[ASN][1000 genomes]
rs6730096	0.84[EUR][1000 genomes]
rs67324207	0.98[ASN][1000 genomes]
rs6735839	0.85[ASN][1000 genomes]
rs6749420	0.85[ASN][1000 genomes]
rs6749586	0.98[ASN][1000 genomes]
rs68056256	0.98[ASN][1000 genomes]
rs72901564	0.98[ASN][1000 genomes]
rs72901581	0.98[ASN][1000 genomes]
rs72903517	0.94[ASN][1000 genomes]
rs72903530	0.85[ASN][1000 genomes]
rs72907635	0.80[ASN][1000 genomes]
rs73034491	0.82[ASN][1000 genomes]
rs73034500	0.82[ASN][1000 genomes]
rs73034501	0.82[ASN][1000 genomes]
rs73036412	0.82[ASN][1000 genomes]
rs73039927	0.98[ASN][1000 genomes]
rs73039929	0.98[ASN][1000 genomes]
rs73041656	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73043732	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7559554	0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs7562160	0.80[ASN][1000 genomes]
rs7577265	0.80[ASN][1000 genomes]
rs7586536	0.98[ASN][1000 genomes]
rs7596399	0.98[ASN][1000 genomes]
rs7601023	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs9653312	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs980065	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[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	nsv1010394	chr2:188994398-189284092	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
2	nsv998395	chr2:189018246-189284092	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv431879	chr2:189079494-189118494	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr2:189100400-189121200	Weak transcription	K562	blood
2	chr2:189108400-189110000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:189108400-189110600	Enhancers	HMEC	breast
4	chr2:189108800-189109400	Enhancers	HUES64 Cell Line	embryonic stem cell

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