Variant report

Variant	rs10857506
Chromosome Location	chr10:50761395-50761396
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:50760936..50763303-chr10:50765007..50767673,2	K562	blood:
2	chr10:50760373..50763303-chr10:50765007..50769387,4	K562	blood:
3	chr10:50760754..50763367-chr10:50770167..50772403,2	MCF-7	breast:

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10776575	0.85[EUR][1000 genomes]
rs10776581	0.91[ASN][1000 genomes]
rs10776583	0.81[EUR][1000 genomes]
rs10857504	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10857510	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11101144	0.81[ASN][1000 genomes]
rs11101155	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11591393	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12146288	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1917803	0.81[ASN][1000 genomes]
rs1917820	0.82[EUR][1000 genomes]
rs1917821	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2177819	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2229760	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2281792	0.81[ASN][1000 genomes]
rs2281793	0.81[ASN][1000 genomes]
rs2377900	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3750747	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs3793784	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4253038	0.86[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4253160	0.81[AMR][1000 genomes]
rs4253190	0.82[AMR][1000 genomes]
rs4253234	0.84[EUR][1000 genomes]
rs6537540	0.91[ASN][1000 genomes]
rs7081472	0.91[ASN][1000 genomes]
rs7895633	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7898545	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9971208	0.81[ASN][1000 genomes]
rs9988727	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[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	nsv895375	chr10:50306386-51028871	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
2	nsv534410	chr10:50317458-50826916	Weak transcription Bivalent Enhancer Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv831867	chr10:50607857-50788751	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	esv3346476	chr10:50610853-50987802	Bivalent/Poised TSS Bivalent Enhancer Active TSS Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
5	esv3385048	chr10:50610942-50988537	Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:50756200-50761400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr10:50756400-50762000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr10:50757200-50763400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr10:50757400-50763000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr10:50757400-50763200	Enhancers	NHEK	skin
6	chr10:50757400-50763400	Enhancers	HMEC	breast
7	chr10:50757800-50761400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:50759200-50761400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr10:50760400-50762000	Enhancers	Osteobl	bone
10	chr10:50760400-50763400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr10:50760400-50765600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr10:50760600-50767400	Weak transcription	HSMMtube	muscle
13	chr10:50760800-50761400	Flanking Active TSS	Hela-S3	cervix
14	chr10:50760800-50761600	Enhancers	Placenta Amnion	Placenta Amnion
15	chr10:50760800-50761600	Enhancers	HSMM	muscle
16	chr10:50760800-50761800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr10:50761000-50761800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr10:50761000-50762600	Enhancers	HUVEC	blood vessel
19	chr10:50761000-50764600	Weak transcription	NHDF-Ad	bronchial
20	chr10:50761200-50761400	Enhancers	Aorta	Aorta
21	chr10:50761200-50762400	Enhancers	Muscle Satellite Cultured Cells	--

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