Variant report

Variant	rs12931678
Chromosome Location	chr16:80994030-80994031
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	chr16:80992093..80994381-chr16:81038938..81040889,2	MCF-7	breast:
2	chr16:80992891..80995365-chr16:80995391..80997695,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000166451	Chromatin interaction
ENSG00000103121	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs11866124	1.00[CHB][hapmap]
rs12444974	1.00[CHB][hapmap]
rs12918103	1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12919463	1.00[EUR][1000 genomes]
rs12919980	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12920066	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12921900	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12921990	1.00[EUR][1000 genomes]
rs12922449	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12924576	0.88[ASN][1000 genomes]
rs12924715	1.00[EUR][1000 genomes]
rs12924719	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12928381	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12928648	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12928790	1.00[EUR][1000 genomes]
rs12929250	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12930046	1.00[AFR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12930202	1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12931555	1.00[EUR][1000 genomes]
rs12931766	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12931852	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12932119	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12932272	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12932466	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs12933920	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13329702	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13333603	1.00[EUR][1000 genomes]
rs13336113	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16954505	1.00[CHB][hapmap]
rs2241408	1.00[EUR][1000 genomes]
rs2278021	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs2278023	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2303214	1.00[CHB][hapmap];1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2549893	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs28838915	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34075739	1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs34082687	1.00[EUR][1000 genomes]
rs34105513	1.00[EUR][1000 genomes]
rs34262209	1.00[EUR][1000 genomes]
rs34270219	1.00[EUR][1000 genomes]
rs34277507	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34529307	1.00[EUR][1000 genomes]
rs34545373	1.00[EUR][1000 genomes]
rs34586837	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34638844	1.00[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34699659	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs34966856	1.00[EUR][1000 genomes]
rs34984547	0.91[ASN][1000 genomes]
rs34992819	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs35011155	1.00[EUR][1000 genomes]
rs35035454	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35110550	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35117857	1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35161190	1.00[EUR][1000 genomes]
rs35282277	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35292442	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35552248	1.00[EUR][1000 genomes]
rs35674322	1.00[EUR][1000 genomes]
rs35887664	1.00[EUR][1000 genomes]
rs35890164	1.00[EUR][1000 genomes]
rs35899445	1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs36040615	1.00[EUR][1000 genomes]
rs36052656	1.00[EUR][1000 genomes]
rs36056886	1.00[EUR][1000 genomes]
rs36099793	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3759931	1.00[EUR][1000 genomes]
rs4889233	1.00[CHB][hapmap]
rs5023849	1.00[CHB][hapmap]
rs57203494	1.00[EUR][1000 genomes]
rs6420421	1.00[CHB][hapmap]
rs71400131	1.00[EUR][1000 genomes]
rs71400134	1.00[EUR][1000 genomes]
rs71400135	1.00[EUR][1000 genomes]
rs71400136	1.00[EUR][1000 genomes]
rs71400137	1.00[EUR][1000 genomes]
rs71400138	1.00[EUR][1000 genomes]
rs71400140	1.00[EUR][1000 genomes]
rs71400141	1.00[EUR][1000 genomes]
rs71400142	1.00[EUR][1000 genomes]
rs7200400	0.89[EUR][1000 genomes]
rs7202356	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs73582605	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs754428	0.89[EUR][1000 genomes]
rs804893	1.00[EUR][1000 genomes]
rs8049484	0.81[ASN][1000 genomes]
rs8049650	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs8062810	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8177862	1.00[EUR][1000 genomes]
rs8177863	1.00[EUR][1000 genomes]
rs8177878	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs8177891	1.00[CHB][hapmap];1.00[EUR][1000 genomes]
rs8177919	1.00[EUR][1000 genomes]
rs8177938	1.00[EUR][1000 genomes]
rs874051	0.97[ASN][1000 genomes]
rs9922227	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9930427	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3451298	chr16:80696935-80997389	Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	esv3350075	chr16:80696955-80997359	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv948534	chr16:80867635-81160492	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
4	nsv1065258	chr16:80887483-81081768	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
5	nsv1058045	chr16:80918138-81048242	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
6	nsv1064164	chr16:80918138-81126967	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats 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
7	nsv542991	chr16:80918138-81126967	Weak transcription Strong transcription Transcr. at gene 5' and 3' Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
8	nsv1067066	chr16:80954876-80996272	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
9	nsv1059905	chr16:80954876-80998523	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
10	esv2760441	chr16:80954888-80998523	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
11	nsv520122	chr16:80955393-81001915	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
12	nsv907004	chr16:80958442-81001915	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
13	nsv1067350	chr16:80959475-80996272	Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
14	nsv1058131	chr16:80967367-80998523	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
15	esv2756816	chr16:80972279-81027142	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
16	esv2758663	chr16:80972279-81027142	Enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
17	nsv532569	chr16:80980356-81700149	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
18	nsv817744	chr16:80989859-81027685	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:80989400-81008800	Weak transcription	Gastric	stomach

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