Variant report

Variant	rs12635427
Chromosome Location	chr3:163626652-163626653
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:82)

rs_ID	r²[population]
rs10936370	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10936371	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10936374	0.89[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10936375	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11706738	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11712177	0.82[ASN][1000 genomes]
rs11922236	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11922757	0.84[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs11926849	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs12635319	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13062126	0.80[ASN][1000 genomes]
rs13077977	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13078251	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13084051	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13094562	0.84[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs13100258	0.88[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1358968	0.80[ASN][1000 genomes]
rs1575352	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1575353	0.87[ASN][1000 genomes]
rs1575355	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1575356	0.80[ASN][1000 genomes]
rs2087823	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2365539	0.83[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2365540	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2365541	0.80[ASN][1000 genomes]
rs2365542	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs2365597	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs34518315	0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3843868	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3843869	0.82[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs3843870	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3849453	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3849455	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs3849457	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs3849461	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3849465	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs3849466	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs3860531	0.88[ASN][1000 genomes]
rs3889963	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3903745	0.80[ASN][1000 genomes]
rs3903760	0.82[ASN][1000 genomes]
rs3903762	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3903763	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3903766	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3903767	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3908413	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs3908414	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs3915750	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs3926030	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs3926031	0.85[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs3934214	0.82[ASN][1000 genomes]
rs3961638	0.80[ASN][1000 genomes]
rs3974998	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs3974999	0.80[ASN][1000 genomes]
rs3975003	0.80[ASN][1000 genomes]
rs3975005	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4254663	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs4266197	0.81[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6548304	0.83[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6774001	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs6781324	0.92[ASN][1000 genomes]
rs6788991	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6791822	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6799984	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs6810275	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7625153	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7628391	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7630237	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs7645490	0.85[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs7649765	0.84[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9829001	0.82[ASN][1000 genomes]
rs9829413	0.81[ASN][1000 genomes]
rs9829526	0.82[ASN][1000 genomes]
rs9830106	0.81[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs9830192	0.81[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs9833823	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs9833882	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs9834984	0.86[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9835488	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs9839780	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs9843404	0.85[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs9860380	0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003820	chr3:163133455-163675884	Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv536788	chr3:163133455-163675884	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv877812	chr3:163313230-163747389	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv877814	chr3:163313230-163758210	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv877813	chr3:163313230-163761825	Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv877816	chr3:163323028-163758210	Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv877819	chr3:163365504-163719054	Enhancers ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv1011576	chr3:163378461-163694975	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
9	nsv1001892	chr3:163410640-163799676	Active TSS Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv536789	chr3:163410640-163799676	Bivalent Enhancer ZNF genes & repeats Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv829780	chr3:163526388-163678908	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
12	nsv877820	chr3:163557163-164167085	Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
13	nsv999377	chr3:163587339-163639942	Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
14	nsv829781	chr3:163600633-163761895	Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	esv2757903	chr3:163602449-163910060	Enhancers ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
16	esv2759199	chr3:163602449-163910060	Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
17	nsv428097	chr3:163602449-163910060	Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
18	nsv428425	chr3:163602449-163910060	Weak transcription Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
19	nsv877822	chr3:163617092-163719054	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
20	nsv877823	chr3:163620918-163671071	Genic enhancers Enhancers Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv877824	chr3:163620918-163728076	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
22	nsv877825	chr3:163620918-164126802	Flanking Active TSS Active TSS ZNF genes & repeats Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163625200-163628400	Active TSS	iPS-18 Cell Line	embryonic stem cell
2	chr3:163626200-163627000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
3	chr3:163626600-163627600	Active TSS	HUES6 Cell Line	embryonic stem cell

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