Variant report

Variant	rs11918635
Chromosome Location	chr3:155151836-155151837
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs11915975	1.00[MEX][hapmap]
rs11925808	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs11928539	1.00[CEU][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16824965	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16824986	1.00[GIH][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16824992	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16825048	1.00[CEU][hapmap]
rs28503947	1.00[ASN][1000 genomes]
rs34828234	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4302412	1.00[ASN][1000 genomes]
rs4352412	1.00[ASN][1000 genomes]
rs4352413	1.00[ASN][1000 genomes]
rs4392458	1.00[ASN][1000 genomes]
rs4630983	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs57461710	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57825069	1.00[ASN][1000 genomes]
rs57985049	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58523386	1.00[ASN][1000 genomes]
rs6440982	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs6440983	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs6440984	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs6764943	1.00[CEU][hapmap]
rs6777732	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs6791188	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs6791222	1.00[CEU][hapmap];1.00[ASN][1000 genomes]
rs6802130	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs6802336	1.00[ASN][1000 genomes]
rs6805227	1.00[ASN][1000 genomes]
rs73009792	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011512	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011513	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011515	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73011525	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73873187	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7637223	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999994	chr3:154579254-155175303	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv532664	chr3:154588346-155162615	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
3	nsv1000753	chr3:154848433-155207022	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv536773	chr3:154848433-155207022	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	nsv877679	chr3:155128968-155204939	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:155151600-155152600	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr3:155151600-155152600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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