Variant report

Variant	rs62436813
Chromosome Location	chr2:78193350-78193351
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 100 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1077890	0.85[ASN][1000 genomes]
rs1105955	0.84[ASN][1000 genomes]
rs1105956	0.81[ASN][1000 genomes]
rs11154374	0.83[ASN][1000 genomes]
rs11154375	0.84[ASN][1000 genomes]
rs11154376	0.84[ASN][1000 genomes]
rs11154377	0.84[ASN][1000 genomes]
rs11154378	0.84[ASN][1000 genomes]
rs11752270	0.89[ASN][1000 genomes]
rs11752287	0.92[ASN][1000 genomes]
rs11754167	0.90[ASN][1000 genomes]
rs11754682	0.89[ASN][1000 genomes]
rs11755390	0.86[ASN][1000 genomes]
rs11756347	0.90[ASN][1000 genomes]
rs11759735	0.85[ASN][1000 genomes]
rs12173960	0.80[ASN][1000 genomes]
rs12234117	0.84[ASN][1000 genomes]
rs12234163	0.84[ASN][1000 genomes]
rs12664316	0.84[ASN][1000 genomes]
rs13190766	0.89[ASN][1000 genomes]
rs13201060	0.91[ASN][1000 genomes]
rs13201789	0.88[ASN][1000 genomes]
rs13204751	0.84[ASN][1000 genomes]
rs13207064	0.89[ASN][1000 genomes]
rs13207638	0.89[ASN][1000 genomes]
rs13213649	0.84[ASN][1000 genomes]
rs13215166	0.91[ASN][1000 genomes]
rs13216524	0.88[ASN][1000 genomes]
rs1361831	0.85[ASN][1000 genomes]
rs1539554	0.85[ASN][1000 genomes]
rs1539556	0.85[ASN][1000 genomes]
rs1543705	0.86[ASN][1000 genomes]
rs1543706	0.86[ASN][1000 genomes]
rs1543707	0.86[ASN][1000 genomes]
rs17570053	0.89[ASN][1000 genomes]
rs1832986	0.86[ASN][1000 genomes]
rs1930942	0.86[ASN][1000 genomes]
rs1930943	0.86[ASN][1000 genomes]
rs1930944	0.86[ASN][1000 genomes]
rs3195537	0.84[ASN][1000 genomes]
rs34072374	0.85[ASN][1000 genomes]
rs34443655	0.89[ASN][1000 genomes]
rs34656055	0.91[ASN][1000 genomes]
rs34937037	0.82[ASN][1000 genomes]
rs35108222	0.84[ASN][1000 genomes]
rs35697500	0.84[ASN][1000 genomes]
rs35870379	0.83[ASN][1000 genomes]
rs35900147	0.91[ASN][1000 genomes]
rs35944960	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs3926855	0.83[ASN][1000 genomes]
rs58274947	0.84[ASN][1000 genomes]
rs59540076	0.89[ASN][1000 genomes]
rs62426327	0.88[ASN][1000 genomes]
rs62439171	0.84[ASN][1000 genomes]
rs62439174	0.84[ASN][1000 genomes]
rs62439175	0.83[ASN][1000 genomes]
rs62439176	0.84[ASN][1000 genomes]
rs6902861	0.85[ASN][1000 genomes]
rs6908014	0.85[ASN][1000 genomes]
rs6920370	0.86[ASN][1000 genomes]
rs6921132	0.86[ASN][1000 genomes]
rs6940295	0.86[ASN][1000 genomes]
rs6940442	0.81[ASN][1000 genomes]
rs6941106	0.86[ASN][1000 genomes]
rs7739746	0.83[ASN][1000 genomes]
rs7745882	0.86[ASN][1000 genomes]
rs7746534	0.86[ASN][1000 genomes]
rs7753502	0.84[ASN][1000 genomes]
rs7758037	0.84[ASN][1000 genomes]
rs7766269	0.86[ASN][1000 genomes]
rs9372845	0.88[ASN][1000 genomes]
rs9372849	0.86[ASN][1000 genomes]
rs9372850	0.84[ASN][1000 genomes]
rs9372851	0.81[ASN][1000 genomes]
rs9375459	0.88[ASN][1000 genomes]
rs9375460	0.84[ASN][1000 genomes]
rs9375472	0.91[ASN][1000 genomes]
rs9375474	0.89[ASN][1000 genomes]
rs9375477	0.81[ASN][1000 genomes]
rs9385410	0.86[ASN][1000 genomes]
rs9388530	0.88[ASN][1000 genomes]
rs9388535	0.91[ASN][1000 genomes]
rs9388537	0.85[ASN][1000 genomes]
rs9398821	0.91[ASN][1000 genomes]
rs9398822	0.89[ASN][1000 genomes]
rs9398823	0.86[ASN][1000 genomes]
rs9401912	0.88[ASN][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	nsv874345	chr2:77912770-78199268	Enhancers Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv917204	chr2:78047538-78602013	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	esv3329151	chr2:78071300-78271485	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1003166	chr2:78091352-78211828	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv1001461	chr2:78091352-78673948	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	esv2757811	chr2:78126389-78711032	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv2759068	chr2:78126389-78711032	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1003010	chr2:78145703-78219800	Active TSS Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv1010580	chr2:78171642-78206296	Weak transcription Enhancers Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv1000527	chr2:78176225-78468796	Enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	esv3449162	chr2:78181346-78221434	Weak transcription Active TSS Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	esv3404781	chr2:78186346-78220877	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
13	esv3447123	chr2:78186346-78239095	Weak transcription Enhancers Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:78193200-78195000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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