Variant report

Variant	rs12901860
Chromosome Location	chr15:51189326-51189327
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:51187671..51190054-chr15:51190212..51192849,2	K562	blood:
2	chr15:51188372..51190064-chr15:51192876..51195738,3	K562	blood:
3	chr15:51186902..51189872-chr15:51192876..51194518,2	K562	blood:

Extended variants
information (count: 118 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:104)

rs_ID	r²[population]
rs10152336	0.80[EUR][1000 genomes]
rs10153007	0.80[EUR][1000 genomes]
rs11070825	0.93[CEU][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11854559	0.80[EUR][1000 genomes]
rs11854729	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11856129	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11857981	0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12324214	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs12324583	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs12898402	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs12899397	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12899528	0.80[EUR][1000 genomes]
rs12902196	0.94[EUR][1000 genomes]
rs12904155	0.93[CEU][hapmap];0.81[EUR][1000 genomes]
rs12906205	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs12907367	0.93[CEU][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12909780	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12911270	0.93[CEU][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12913094	0.89[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12916334	0.94[EUR][1000 genomes]
rs1438926	0.93[CEU][hapmap];0.81[EUR][1000 genomes]
rs16953045	0.93[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16963910	0.80[EUR][1000 genomes]
rs16963912	0.80[EUR][1000 genomes]
rs16963947	0.80[EUR][1000 genomes]
rs17521467	0.93[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17521789	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17521919	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17599863	0.93[CEU][hapmap];1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs17599974	0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1904432	0.92[CEU][hapmap];0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1912097	0.86[CEU][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2083254	0.84[EUR][1000 genomes]
rs2306333	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2414053	0.83[EUR][1000 genomes]
rs2414054	0.83[EUR][1000 genomes]
rs2414055	0.80[EUR][1000 genomes]
rs2414056	0.80[EUR][1000 genomes]
rs28366661	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28430533	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28566562	0.80[EUR][1000 genomes]
rs28642856	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2899459	0.83[EUR][1000 genomes]
rs34293575	0.82[EUR][1000 genomes]
rs34297767	0.80[EUR][1000 genomes]
rs34575622	0.80[EUR][1000 genomes]
rs34581168	0.80[EUR][1000 genomes]
rs34676299	0.80[EUR][1000 genomes]
rs34874493	0.84[EUR][1000 genomes]
rs35114758	0.81[EUR][1000 genomes]
rs35134521	0.82[EUR][1000 genomes]
rs35416047	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35439349	0.94[EUR][1000 genomes]
rs35464909	0.80[EUR][1000 genomes]
rs35655196	0.84[EUR][1000 genomes]
rs35845857	0.80[EUR][1000 genomes]
rs3759806	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3848133	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs3848134	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs3848135	0.80[EUR][1000 genomes]
rs3896066	0.80[EUR][1000 genomes]
rs3925824	0.80[EUR][1000 genomes]
rs3929486	0.80[EUR][1000 genomes]
rs4134038	0.94[EUR][1000 genomes]
rs4344678	0.84[EUR][1000 genomes]
rs4402498	0.82[EUR][1000 genomes]
rs4451894	0.83[EUR][1000 genomes]
rs58661036	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6493459	0.80[EUR][1000 genomes]
rs71471517	0.80[EUR][1000 genomes]
rs71471522	0.94[EUR][1000 genomes]
rs71471523	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs71471584	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs71471585	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71471587	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7162325	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs7162631	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs7165920	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7166073	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7166600	0.94[EUR][1000 genomes]
rs7169887	0.80[EUR][1000 genomes]
rs7170009	0.93[CEU][hapmap];0.84[EUR][1000 genomes]
rs7170364	0.80[EUR][1000 genomes]
rs7170937	0.87[CEU][hapmap];0.80[EUR][1000 genomes]
rs7172667	0.80[EUR][1000 genomes]
rs7175024	0.93[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7179321	0.86[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7179865	0.86[CEU][hapmap];0.80[EUR][1000 genomes]
rs8023655	0.82[EUR][1000 genomes]
rs8024423	0.80[EUR][1000 genomes]
rs8024689	0.83[EUR][1000 genomes]
rs8024733	0.80[EUR][1000 genomes]
rs8029786	0.80[EUR][1000 genomes]
rs8032236	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs8032550	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8032866	0.93[CEU][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs8033307	0.80[EUR][1000 genomes]
rs8033351	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs8033471	0.80[EUR][1000 genomes]
rs8034303	0.80[EUR][1000 genomes]
rs8034718	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs9302158	0.93[CEU][hapmap];0.80[EUR][1000 genomes]
rs9630423	0.80[EUR][1000 genomes]
rs9806654	0.93[CEU][hapmap];0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
3	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
5	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
7	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
8	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
9	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
10	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
11	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
12	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
13	nsv516168	chr15:51114437-51217361	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
14	nsv428636	chr15:51154834-51298044	Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51177800-51199200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr15:51177800-51199600	Weak transcription	Ovary	ovary
3	chr15:51179000-51199200	Weak transcription	Brain Angular Gyrus	brain
4	chr15:51183800-51199200	Weak transcription	Brain Substantia Nigra	brain
5	chr15:51185800-51199800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr15:51187200-51199000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:51187200-51199200	Weak transcription	Placenta	Placenta
8	chr15:51188400-51199200	Weak transcription	Fetal Lung	lung

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