Variant report

Variant	rs2596156
Chromosome Location	chr15:33742178-33742179
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs1155606	0.90[CHB][hapmap];0.90[ASN][1000 genomes]
rs1560968	0.91[ASW][hapmap];0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.81[JPT][hapmap];0.82[MKK][hapmap];0.80[TSI][hapmap];0.85[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs1878298	1.00[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.93[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1878299	0.89[CEU][hapmap];0.95[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2339275	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2459470	0.90[CHB][hapmap];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2572192	0.81[CEU][hapmap];0.90[CHB][hapmap];0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2572193	0.91[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2596157	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2596236	0.86[CHB][hapmap];0.88[CHD][hapmap];0.84[JPT][hapmap];0.84[ASN][1000 genomes]
rs2676017	0.84[CEU][hapmap];0.90[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs2676085	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.89[GIH][hapmap];0.90[MEX][hapmap];0.84[TSI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2676086	0.83[ASW][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];0.87[ASN][1000 genomes]
rs2676087	1.00[ASW][hapmap];0.90[CHB][hapmap];1.00[CHD][hapmap];0.85[MKK][hapmap];0.85[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2676088	0.90[CHB][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs2676089	0.90[CHB][hapmap];0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs2676090	0.85[CEU][hapmap];0.90[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs2676096	0.80[AMR][1000 genomes]
rs7165065	0.86[CHB][hapmap];0.88[CHD][hapmap];0.82[ASN][1000 genomes]
rs930300	0.90[CHB][hapmap];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533346	chr15:33469439-33809641	Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv832964	chr15:33608771-33784018	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv1043046	chr15:33714908-34321330	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	esv34041	chr15:33720726-33871487	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	esv34037	chr15:33732616-34049083	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33732800-33746600	Weak transcription	Aorta	Aorta
2	chr15:33733400-33746000	Weak transcription	Brain Anterior Caudate	brain
3	chr15:33740000-33743400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr15:33740200-33742200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr15:33740200-33742200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr15:33740400-33744600	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr15:33740800-33742200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:33740800-33742400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr15:33740800-33743400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr15:33740800-33744400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr15:33741000-33742200	Enhancers	Esophagus	oesophagus
12	chr15:33741000-33743200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:33741000-33744400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:33741200-33742200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:33741200-33742800	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr15:33741400-33743000	Weak transcription	Pancreas	Pancrea
17	chr15:33741600-33744600	Enhancers	NHEK	skin
18	chr15:33741600-33765400	Weak transcription	Fetal Muscle Leg	muscle
19	chr15:33741800-33742400	Enhancers	HMEC	breast
20	chr15:33741800-33742800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr15:33742000-33742200	Enhancers	Primary hematopoietic stem cells	blood
22	chr15:33742000-33742200	Flanking Active TSS	Fetal Kidney	kidney

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