Variant report

Variant	rs35589072
Chromosome Location	chr2:46733915-46733916
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:46733619..46735198-chr2:46736936..46739101,2	K562	blood:
2	chr2:46733777..46735445-chr2:46737259..46739912,2	MCF-7	breast:
3	chr2:46534025..46536338-chr2:46732082..46734041,2	K562	blood:
4	chr2:46733615..46735583-chr2:46736562..46738706,2	K562	blood:
5	chr2:46733223..46735001-chr2:46740997..46743656,2	MCF-7	breast:

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs11125078	0.80[EUR][1000 genomes]
rs11125081	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12470939	0.80[EUR][1000 genomes]
rs12471274	0.89[EUR][1000 genomes]
rs12473673	0.83[EUR][1000 genomes]
rs12474965	0.83[EUR][1000 genomes]
rs12612916	0.83[EUR][1000 genomes]
rs12613088	0.83[EUR][1000 genomes]
rs12613600	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12617193	0.92[EUR][1000 genomes]
rs12619386	0.86[EUR][1000 genomes]
rs12619696	0.92[EUR][1000 genomes]
rs12619754	0.80[EUR][1000 genomes]
rs12621486	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12622818	0.83[EUR][1000 genomes]
rs1530623	0.80[EUR][1000 genomes]
rs1551123	0.86[EUR][1000 genomes]
rs1562454	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17035200	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1868845	0.83[EUR][1000 genomes]
rs2053766	0.80[EUR][1000 genomes]
rs2121699	0.86[EUR][1000 genomes]
rs2166746	0.80[EUR][1000 genomes]
rs2276556	0.83[EUR][1000 genomes]
rs34405528	0.83[EUR][1000 genomes]
rs4145835	0.80[EUR][1000 genomes]
rs4952826	0.83[EUR][1000 genomes]
rs4952827	0.83[EUR][1000 genomes]
rs4953364	0.83[EUR][1000 genomes]
rs4953370	0.80[EUR][1000 genomes]
rs4953376	0.80[EUR][1000 genomes]
rs4953395	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs55871716	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56894248	0.92[EUR][1000 genomes]
rs57996107	0.89[EUR][1000 genomes]
rs58402726	0.86[EUR][1000 genomes]
rs58725320	0.86[EUR][1000 genomes]
rs59013670	0.83[EUR][1000 genomes]
rs59761895	0.86[EUR][1000 genomes]
rs59856996	0.92[EUR][1000 genomes]
rs60685999	0.92[EUR][1000 genomes]
rs61193538	0.89[EUR][1000 genomes]
rs66533451	0.89[EUR][1000 genomes]
rs6714240	0.80[EUR][1000 genomes]
rs6723195	0.83[EUR][1000 genomes]
rs67739992	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67960524	0.92[EUR][1000 genomes]
rs68030749	0.89[EUR][1000 genomes]
rs72618622	0.80[EUR][1000 genomes]
rs72618623	0.80[EUR][1000 genomes]
rs72618624	0.80[EUR][1000 genomes]
rs72618625	0.80[EUR][1000 genomes]
rs72618626	0.80[EUR][1000 genomes]
rs72618627	0.80[EUR][1000 genomes]
rs72618628	0.86[EUR][1000 genomes]
rs72618629	0.86[EUR][1000 genomes]
rs72618631	0.83[EUR][1000 genomes]
rs72618632	0.86[EUR][1000 genomes]
rs72873772	0.89[EUR][1000 genomes]
rs7573688	0.80[EUR][1000 genomes]
rs7574467	0.80[EUR][1000 genomes]
rs7595513	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012446	chr2:45921682-46737036	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv2757795	chr2:46532812-46874151	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	esv2759046	chr2:46532812-46874151	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
4	esv34650	chr2:46605659-46818992	Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	esv2756919	chr2:46614235-46756431	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
6	nsv437435	chr2:46636967-46763587	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
7	esv34937	chr2:46651624-46818586	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
8	nsv9702	chr2:46668106-46745740	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv817828	chr2:46670146-46739157	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv1014425	chr2:46670179-47033417	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Genic enhancers 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 miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv535678	chr2:46670179-47033417	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
12	nsv873996	chr2:46670941-47065227	Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
13	nsv1009735	chr2:46724523-46913152	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46727600-46738200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr2:46731400-46736800	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr2:46732200-46735000	Weak transcription	K562	blood
4	chr2:46732800-46734400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:46733000-46734000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr2:46733000-46734200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
7	chr2:46733000-46734400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:46733200-46734000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr2:46733200-46734200	Enhancers	Primary hematopoietic stem cells short term culture	blood
10	chr2:46733400-46734000	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr2:46733800-46753000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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