Variant report

Variant	rs2705728
Chromosome Location	chr2:183969305-183969306
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	chr2:183967945..183970518-chr2:183975860..183978004,2	K562	blood:
2	chr2:183961564..183963218-chr2:183968375..183970375,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs11684034	0.84[AMR][1000 genomes]
rs2138483	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2176227	1.00[CEU][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2248705	0.84[AMR][1000 genomes]
rs2254867	0.80[AMR][1000 genomes]
rs2459336	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2675043	0.80[CEU][hapmap];1.00[CHD][hapmap];0.81[YRI][hapmap];1.00[ASN][1000 genomes]
rs2675059	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2675064	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675066	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675070	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675080	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2675081	0.84[AMR][1000 genomes]
rs2675100	0.84[AMR][1000 genomes]
rs2675103	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2705711	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2705717	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2705725	0.82[MEX][hapmap];0.86[TSI][hapmap]
rs2705726	0.82[MEX][hapmap];0.86[TSI][hapmap]
rs2705731	1.00[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2705733	1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs2705738	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2705761	0.84[AMR][1000 genomes]
rs2705764	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2887233	0.82[MEX][hapmap];0.86[TSI][hapmap];0.84[AMR][1000 genomes]
rs4666616	0.84[AMR][1000 genomes]
rs4666618	0.84[AMR][1000 genomes]
rs6434012	0.84[AMR][1000 genomes]
rs6434018	0.84[AMR][1000 genomes]
rs6751275	0.84[AMR][1000 genomes]
rs72890368	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72896587	0.84[AMR][1000 genomes]
rs72896589	0.84[AMR][1000 genomes]
rs72896592	0.84[AMR][1000 genomes]
rs72896594	0.84[AMR][1000 genomes]
rs72898506	0.84[AMR][1000 genomes]
rs72898520	0.84[AMR][1000 genomes]
rs72898559	0.84[AMR][1000 genomes]
rs7355427	0.84[AMR][1000 genomes]
rs7420841	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 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	nsv1005281	chr2:183803173-184093877	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	nsv1003519	chr2:183885544-184015868	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	esv2763287	chr2:183939173-184037893	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	esv3356302	chr2:183962495-183989877	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:183945800-183972600	Weak transcription	Stomach Smooth Muscle	stomach
2	chr2:183954600-183988400	Weak transcription	Aorta	Aorta
3	chr2:183959400-183970200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr2:183968200-183970600	Enhancers	Muscle Satellite Cultured Cells	--

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