Variant report

Variant	rs186736
Chromosome Location	chr2:179053468-179053469
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:179047545..179050126-chr2:179052607..179054172,2	K562	blood:
2	chr2:179052165..179056550-chr2:179057804..179060174,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000079156	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10187205	0.83[ASN][1000 genomes]
rs10197166	0.86[JPT][hapmap]
rs10930827	0.87[JPT][hapmap]
rs12185670	0.82[JPT][hapmap]
rs12471750	0.85[ASN][1000 genomes]
rs12693155	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs13389850	0.89[ASN][1000 genomes]
rs17638592	0.93[ASN][1000 genomes]
rs232042	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2366157	0.86[JPT][hapmap]
rs2366365	0.82[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs3099472	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs333996	0.86[JPT][hapmap]
rs334005	0.86[JPT][hapmap]
rs334007	0.86[JPT][hapmap]
rs334017	0.86[JPT][hapmap]
rs334024	0.87[JPT][hapmap]
rs334028	0.86[JPT][hapmap]
rs334035	0.86[JPT][hapmap]
rs334037	0.87[JPT][hapmap]
rs334040	0.86[JPT][hapmap]
rs334042	0.86[JPT][hapmap]
rs334045	0.86[JPT][hapmap]
rs334079	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs334080	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs334081	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs334092	0.88[ASN][1000 genomes]
rs334094	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs334102	0.83[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.87[MEX][hapmap];0.94[ASN][1000 genomes]
rs334103	0.82[CHB][hapmap];0.91[CHD][hapmap];0.93[JPT][hapmap];0.87[MEX][hapmap];0.94[ASN][1000 genomes]
rs334110	0.93[JPT][hapmap]
rs334115	0.85[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs334116	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs334117	0.85[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs334122	0.94[ASN][1000 genomes]
rs334125	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs334126	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs334128	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs334132	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs334133	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs437523	0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs4894001	0.87[ASN][1000 genomes]
rs6719178	0.86[JPT][hapmap]
rs7419749	0.87[JPT][hapmap]
rs7581504	0.93[JPT][hapmap]
rs7591476	0.87[ASN][1000 genomes]
rs7595650	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs930191	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.82[EUR][1000 genomes];0.87[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	nsv1009312	chr2:178924318-179215566	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv536057	chr2:178924318-179215566	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv875452	chr2:178963445-179167766	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv875453	chr2:179022751-179060313	Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv875454	chr2:179022751-179066443	Bivalent/Poised TSS Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs186736	GPR155	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179037000-179056600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:179052600-179057800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr2:179053400-179053600	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr2:179053400-179053600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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