Variant report

Variant	rs16856261
Chromosome Location	chr2:169803568-169803569
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:169798515..169802093-chr2:169802233..169805225,4	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs1101532	0.82[ASN][1000 genomes]
rs1101533	0.86[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs1101534	0.84[ASN][1000 genomes]
rs1581397	0.85[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs16856252	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2250677	0.84[ASN][1000 genomes]
rs2544360	0.87[ASN][1000 genomes]
rs2544367	0.85[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs2685803	0.83[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs2685804	0.84[ASN][1000 genomes]
rs2685805	0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs2685806	0.84[ASN][1000 genomes]
rs2685807	0.84[ASN][1000 genomes]
rs2685808	0.84[ASN][1000 genomes]
rs2685810	0.84[ASN][1000 genomes]
rs2685811	0.83[ASN][1000 genomes]
rs2685812	0.85[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs2685813	0.85[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs2685814	0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs3755157	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3755158	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs479682	0.85[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs480562	0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs482508	0.84[ASN][1000 genomes]
rs55700007	0.98[AFR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs565412	0.85[CHB][hapmap];0.82[ASN][1000 genomes]
rs567074	0.85[CHB][hapmap]
rs58512362	0.91[AFR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72886761	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs853776	0.85[CHB][hapmap];0.80[ASN][1000 genomes]
rs853778	0.85[CHB][hapmap]
rs853779	0.85[CHB][hapmap];0.83[JPT][hapmap]
rs853780	0.90[CHB][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs853781	0.90[CHB][hapmap];0.82[JPT][hapmap];0.84[ASN][1000 genomes]
rs853782	0.84[ASN][1000 genomes]
rs853783	0.85[CHB][hapmap];0.84[ASN][1000 genomes]
rs853784	0.90[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs853785	0.90[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs853786	0.90[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs853788	0.90[CHB][hapmap];0.83[JPT][hapmap];0.85[ASN][1000 genomes]
rs853790	0.83[ASN][1000 genomes]
rs860510	0.84[ASN][1000 genomes]
rs862662	0.90[CHB][hapmap];0.83[JPT][hapmap]
rs864929	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv583599	chr2:169664227-169903096	Bivalent Enhancer Weak transcription Genic enhancers Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv875382	chr2:169792484-169819824	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1003689	chr2:169797060-169824983	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1000245	chr2:169797060-169830515	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv999345	chr2:169797666-169818302	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1012367	chr2:169797666-169821132	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv459944	chr2:169798619-169893419	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv583601	chr2:169798619-169893419	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	nsv933063	chr2:169801486-169814519	ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:169802600-169803600	Enhancers	Pancreatic Islets	Pancreatic Islet
2	chr2:169802600-169818000	Strong transcription	Liver	Liver

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