Variant report

Variant	rs28600759
Chromosome Location	chr15:55462766-55462767
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10162819	0.90[ASN][1000 genomes]
rs10162843	0.90[ASN][1000 genomes]
rs10518804	0.84[ASN][1000 genomes]
rs1061821	0.81[ASN][1000 genomes]
rs1061874	0.81[ASN][1000 genomes]
rs1061875	0.81[ASN][1000 genomes]
rs11857087	0.83[ASN][1000 genomes]
rs12385963	0.83[ASN][1000 genomes]
rs13733	0.81[ASN][1000 genomes]
rs16976036	0.86[ASN][1000 genomes]
rs16976039	0.86[ASN][1000 genomes]
rs16976065	0.93[ASN][1000 genomes]
rs16976083	0.90[ASN][1000 genomes]
rs16976094	0.91[ASN][1000 genomes]
rs16976116	0.82[ASN][1000 genomes]
rs16976149	0.90[ASN][1000 genomes]
rs28558576	0.91[ASN][1000 genomes]
rs28562431	0.90[ASN][1000 genomes]
rs28592928	0.83[ASN][1000 genomes]
rs28636526	0.84[ASN][1000 genomes]
rs28673043	0.81[ASN][1000 genomes]
rs28706531	0.83[ASN][1000 genomes]
rs28710976	0.83[ASN][1000 genomes]
rs3759861	0.84[ASN][1000 genomes]
rs3759862	0.83[ASN][1000 genomes]
rs3809539	0.85[ASN][1000 genomes]
rs3809540	0.81[ASN][1000 genomes]
rs4238316	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4503734	0.84[ASN][1000 genomes]
rs4545742	0.90[ASN][1000 genomes]
rs6493768	0.83[ASN][1000 genomes]
rs7168472	0.83[ASN][1000 genomes]
rs7179365	0.90[ASN][1000 genomes]
rs7180594	0.90[ASN][1000 genomes]
rs8033588	0.90[ASN][1000 genomes]
rs8034063	0.90[ASN][1000 genomes]
rs8034402	0.83[ASN][1000 genomes]
rs8034853	0.90[ASN][1000 genomes]
rs8034882	0.90[ASN][1000 genomes]
rs8035625	0.83[ASN][1000 genomes]
rs8043029	0.83[ASN][1000 genomes]
rs9300	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043176	chr15:55010228-55563000	Genic enhancers Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1042741	chr15:55068022-55622497	Strong transcription Weak transcription Flanking Active TSS Enhancers 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	31 gene(s)	inside rSNPs	diseases
3	nsv1039471	chr15:55137606-55552555	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
5	nsv457156	chr15:55400649-55466155	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv569521	chr15:55400649-55466155	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 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	chr15:55455600-55469600	Weak transcription	Aorta	Aorta
2	chr15:55455800-55487200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr15:55459000-55469800	Weak transcription	HSMM	muscle
4	chr15:55461000-55469200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:55462600-55463200	Enhancers	A549	lung
6	chr15:55462600-55470200	Weak transcription	Fetal Lung	lung
7	chr15:55462600-55471600	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr15:55462600-55488600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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