Variant report

Variant	rs12622818
Chromosome Location	chr2:46676560-46676561
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF274	chr2:46676542-46677125	K562	blood:	n/a	n/a

Variant related genes	Relation type
RN7SL817P	TF binding region

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs1105595	0.82[CHB][hapmap];0.83[GIH][hapmap];0.93[MEX][hapmap];0.81[ASN][1000 genomes]
rs11125078	0.95[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];0.93[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12470939	0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12471274	0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12472120	0.86[ASN][1000 genomes]
rs12473673	0.94[EUR][1000 genomes]
rs12474961	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12474965	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12475015	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12612916	0.91[CHB][hapmap];0.88[CHD][hapmap];0.94[GIH][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];0.83[TSI][hapmap];0.88[EUR][1000 genomes]
rs12613088	0.91[CHB][hapmap];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12615460	1.00[CEU][hapmap]
rs12617193	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12619386	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12619696	0.91[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];0.90[JPT][hapmap];0.93[MEX][hapmap];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12619754	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12621486	0.84[EUR][1000 genomes]
rs1530623	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[CHD][hapmap];0.89[GIH][hapmap];0.91[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1551123	0.86[MEX][hapmap];0.86[EUR][1000 genomes]
rs1562454	0.86[MEX][hapmap];0.86[EUR][1000 genomes]
rs17035200	0.93[MEX][hapmap];0.83[EUR][1000 genomes]
rs1868090	0.84[ASN][1000 genomes]
rs1868095	0.98[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1868845	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2053766	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2121699	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2166746	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2276556	0.87[CHB][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes]
rs2881326	0.94[EUR][1000 genomes]
rs34405528	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35589072	0.83[EUR][1000 genomes]
rs4145835	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4952825	0.91[CHB][hapmap];0.98[CHD][hapmap];0.89[GIH][hapmap]
rs4952826	0.91[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];0.93[MEX][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes]
rs4952827	0.90[CHB][hapmap];0.85[YRI][hapmap];0.94[EUR][1000 genomes]
rs4953363	1.00[CEU][hapmap]
rs4953364	1.00[CEU][hapmap];0.87[CHB][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4953369	0.83[ASN][1000 genomes]
rs4953370	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4953376	1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4953395	0.83[EUR][1000 genomes]
rs55871716	0.83[EUR][1000 genomes]
rs56894248	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57720200	0.85[ASN][1000 genomes]
rs57996107	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58402726	0.91[EUR][1000 genomes]
rs58725320	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59013670	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs59761895	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59856996	0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60685999	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61193538	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61560601	0.87[ASN][1000 genomes]
rs66533451	0.83[EUR][1000 genomes]
rs6714240	0.82[CHB][hapmap];0.91[EUR][1000 genomes]
rs6723195	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6737959	0.80[CHD][hapmap]
rs67435514	0.83[ASN][1000 genomes]
rs67739992	0.83[EUR][1000 genomes]
rs67960524	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs68030749	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72618620	0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs72618621	0.94[EUR][1000 genomes]
rs72618622	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72618623	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72618624	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72618625	0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs72618626	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72618627	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72618628	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72618629	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72618631	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72618632	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs72873772	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7573688	0.87[CHB][hapmap];0.81[CHD][hapmap];0.93[MEX][hapmap];0.84[MKK][hapmap];0.91[EUR][1000 genomes]
rs7574467	1.00[CEU][hapmap];0.86[CHB][hapmap];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7595513	0.95[CHB][hapmap];0.98[CHD][hapmap];0.94[GIH][hapmap];0.91[JPT][hapmap];0.93[MEX][hapmap];0.80[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 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	nsv997637	chr2:46651624-46676628	Bivalent Enhancer Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv1003646	chr2:46651624-46677186	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	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
10	nsv581745	chr2:46660445-46693963	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	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
12	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
13	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
14	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
15	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

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:46662200-46678400	Weak transcription	Placenta	Placenta
2	chr2:46667000-46688400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr2:46668200-46683600	Weak transcription	K562	blood
4	chr2:46674600-46678400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:46674600-46686600	Weak transcription	NHLF	lung
6	chr2:46675400-46676800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr2:46675400-46677200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr2:46675400-46677200	Enhancers	Hela-S3	cervix
9	chr2:46675600-46678800	Weak transcription	Gastric	stomach
10	chr2:46676200-46676600	Enhancers	Small Intestine	intestine

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