Variant report

Variant	rs2368356
Chromosome Location	chr2:184110466-184110467
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:184109760..184112226-chr2:184112550..184114102,2	K562	blood:
2	chr2:184099257..184101116-chr2:184108671..184111600,2	K562	blood:
3	chr2:184105207..184107780-chr2:184109813..184112746,3	K562	blood:
4	chr2:184103542..184105971-chr2:184110160..184112023,2	MCF-7	breast:
5	chr2:184108494..184111184-chr2:184119007..184120584,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs1037968	0.80[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs11884352	1.00[EUR][1000 genomes]
rs11887082	1.00[EUR][1000 genomes]
rs11889321	1.00[EUR][1000 genomes]
rs11890612	1.00[EUR][1000 genomes]
rs11890957	1.00[EUR][1000 genomes]
rs11898922	1.00[EUR][1000 genomes]
rs11899136	1.00[EUR][1000 genomes]
rs11900146	1.00[EUR][1000 genomes]
rs11904544	1.00[EUR][1000 genomes]
rs1462522	1.00[EUR][1000 genomes]
rs1462523	1.00[EUR][1000 genomes]
rs16823994	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16824047	1.00[CEU][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs16824100	1.00[EUR][1000 genomes]
rs16824103	1.00[EUR][1000 genomes]
rs16824136	1.00[EUR][1000 genomes]
rs16824139	1.00[EUR][1000 genomes]
rs16824141	1.00[EUR][1000 genomes]
rs16824239	1.00[EUR][1000 genomes]
rs16824259	1.00[EUR][1000 genomes]
rs2045760	1.00[EUR][1000 genomes]
rs2061657	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2368374	1.00[EUR][1000 genomes]
rs28807996	1.00[EUR][1000 genomes]
rs34386785	1.00[EUR][1000 genomes]
rs55985024	1.00[EUR][1000 genomes]
rs56987972	1.00[EUR][1000 genomes]
rs57022552	1.00[EUR][1000 genomes]
rs58726290	1.00[EUR][1000 genomes]
rs58782215	1.00[EUR][1000 genomes]
rs59648361	1.00[EUR][1000 genomes]
rs60159376	1.00[EUR][1000 genomes]
rs60835883	1.00[EUR][1000 genomes]
rs60857445	1.00[EUR][1000 genomes]
rs61190837	1.00[EUR][1000 genomes]
rs61212352	1.00[EUR][1000 genomes]
rs6434010	1.00[EUR][1000 genomes]
rs6751386	1.00[EUR][1000 genomes]
rs6759272	1.00[EUR][1000 genomes]
rs73040916	1.00[EUR][1000 genomes]
rs73042731	1.00[EUR][1000 genomes]
rs73042751	1.00[EUR][1000 genomes]
rs73042792	1.00[EUR][1000 genomes]
rs73044730	1.00[EUR][1000 genomes]
rs73050588	1.00[EUR][1000 genomes]
rs73050593	1.00[EUR][1000 genomes]
rs73050598	1.00[EUR][1000 genomes]
rs7584986	1.00[EUR][1000 genomes]
rs898947	1.00[EUR][1000 genomes]
rs955597	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009882	chr2:183213152-184171519	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv875485	chr2:183827018-184195265	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1010799	chr2:183855680-184244721	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
4	nsv536072	chr2:183855680-184244721	Flanking Active TSS Strong transcription ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
5	nsv3067	chr2:184079419-184119957	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
6	nsv1014008	chr2:184085441-184111385	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184108400-184110600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr2:184109600-184114000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:184109600-184114000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr2:184109600-184114000	Weak transcription	HMEC	breast
5	chr2:184109600-184114200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:184109800-184113600	Weak transcription	NHEK	skin

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