Variant report

Variant	rs11250142
Chromosome Location	chr8:11372533-11372534
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11366501..11369054-chr8:11369431..11373497,4	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs11250141	0.87[CHB][hapmap];0.94[JPT][hapmap];0.84[ASN][1000 genomes]
rs11250143	0.95[ASN][1000 genomes]
rs11990277	0.82[CHB][hapmap];0.94[JPT][hapmap];0.83[ASN][1000 genomes]
rs11991127	0.87[JPT][hapmap];0.91[ASN][1000 genomes]
rs12674768	0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs12677903	0.93[JPT][hapmap];0.85[ASN][1000 genomes]
rs1382566	0.82[CHB][hapmap];0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs1478897	0.82[CHB][hapmap];0.94[JPT][hapmap];0.81[ASN][1000 genomes]
rs17153385	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2021819	0.87[ASN][1000 genomes]
rs2248696	0.81[ASN][1000 genomes]
rs2248700	0.81[ASN][1000 genomes]
rs2248932	0.82[CHB][hapmap];0.94[JPT][hapmap];0.85[ASN][1000 genomes]
rs2249259	0.82[JPT][hapmap];0.86[ASN][1000 genomes]
rs2252729	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs2618435	0.86[ASN][1000 genomes]
rs2618437	0.86[ASN][1000 genomes]
rs2618455	0.87[CEU][hapmap];0.86[CHB][hapmap];0.88[JPT][hapmap];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2618456	0.88[CEU][hapmap];0.86[CHB][hapmap];0.89[JPT][hapmap];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2618457	0.87[CEU][hapmap];0.88[EUR][1000 genomes]
rs2618458	0.88[EUR][1000 genomes]
rs2618476	0.81[CHB][hapmap]
rs2729934	0.86[ASN][1000 genomes]
rs2729935	0.86[ASN][1000 genomes]
rs2736353	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2736354	0.87[CEU][hapmap];0.88[EUR][1000 genomes]
rs2736355	0.94[CEU][hapmap];0.88[EUR][1000 genomes]
rs2736356	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2736359	0.93[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.88[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2736360	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2898282	0.89[ASN][1000 genomes]
rs4841546	0.82[ASN][1000 genomes]
rs4841550	0.84[JPT][hapmap];0.83[ASN][1000 genomes]
rs57240873	0.88[ASN][1000 genomes]
rs58373594	0.88[ASN][1000 genomes]
rs62489135	0.84[ASN][1000 genomes]
rs62489136	0.83[ASN][1000 genomes]
rs62489137	0.84[ASN][1000 genomes]
rs6981617	0.81[ASN][1000 genomes]
rs6993775	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7014565	0.93[CHB][hapmap];0.88[JPT][hapmap]
rs73209286	0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73209290	0.87[ASN][1000 genomes]
rs7814834	0.88[JPT][hapmap];0.84[ASN][1000 genomes]
rs7844858	0.86[ASN][1000 genomes]
rs9329246	0.82[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs9657551	0.87[CHB][hapmap];0.94[JPT][hapmap]

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	nsv1035072	chr8:10819444-11480692	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv539473	chr8:10819444-11480692	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv529399	chr8:10970091-11805960	Enhancers Strong transcription Weak transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	esv34097	chr8:11177372-11489894	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
5	nsv1022074	chr8:11292256-11394526	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11357400-11380000	Genic enhancers	Primary B cells from peripheral blood	blood
2	chr8:11365400-11373400	Enhancers	NHEK	skin
3	chr8:11365800-11374600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr8:11366600-11375200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr8:11367000-11373400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:11368200-11372600	Weak transcription	NHLF	lung
7	chr8:11368800-11374600	Enhancers	HSMM	muscle
8	chr8:11368800-11375800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr8:11369200-11372600	Weak transcription	HUVEC	blood vessel
10	chr8:11369400-11372600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr8:11369400-11372600	Weak transcription	NH-A	brain
12	chr8:11369400-11373000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:11369400-11373200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr8:11369600-11372600	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr8:11369600-11372800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr8:11369800-11372600	Weak transcription	NHDF-Ad	bronchial
17	chr8:11370000-11373200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:11370200-11372600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr8:11370200-11375000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr8:11370600-11373600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr8:11370600-11375400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:11370800-11374600	Genic enhancers	Primary B cells from cord blood	blood
23	chr8:11371000-11373800	Enhancers	Sigmoid Colon	Sigmoid Colon
24	chr8:11371200-11372800	Weak transcription	Osteobl	bone
25	chr8:11371400-11372600	Weak transcription	HSMMtube	muscle
26	chr8:11371600-11372600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:11372000-11376000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr8:11372200-11386000	Weak transcription	Spleen	Spleen
29	chr8:11372400-11372600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr8:11372400-11373600	Weak transcription	GM12878-XiMat	blood
31	chr8:11372400-11374800	Enhancers	HMEC	breast

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