Variant report

Variant	rs11782375
Chromosome Location	chr8:11294934-11294935
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:11291994..11295873-chr8:11300373..11305945,6	K562	blood:
2	chr8:11294217..11296027-chr8:11297947..11300867,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000154319	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10088323	0.95[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs10102600	0.86[JPT][hapmap]
rs10448145	0.95[CHB][hapmap];0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs10448146	0.86[ASN][1000 genomes]
rs10481455	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs10503423	0.95[CHB][hapmap];0.85[JPT][hapmap]
rs1057750	0.95[CHB][hapmap];0.90[JPT][hapmap];0.84[ASN][1000 genomes]
rs10903338	0.81[CHB][hapmap]
rs11250136	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11250138	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs11777505	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11779875	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12114115	0.85[CHB][hapmap]
rs12543308	0.85[CHB][hapmap];0.80[JPT][hapmap]
rs12549796	0.95[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap];0.87[ASN][1000 genomes]
rs12674532	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs13259219	0.90[CHB][hapmap]
rs13264212	0.85[CHB][hapmap]
rs13439411	0.81[CHB][hapmap]
rs2003422	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2003423	1.00[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs2280803	0.90[CHB][hapmap];0.81[JPT][hapmap];0.82[ASN][1000 genomes]
rs2409767	0.86[ASN][1000 genomes]
rs2409770	0.86[ASN][1000 genomes]
rs2409771	0.86[ASN][1000 genomes]
rs2409772	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs2409773	0.91[CHB][hapmap];0.80[JPT][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2409775	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs2618431	0.85[CHB][hapmap]
rs2618475	0.81[CHB][hapmap]
rs2736320	0.81[CHB][hapmap]
rs2898279	0.95[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs2898280	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs35161715	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs35433745	0.81[ASN][1000 genomes]
rs3989103	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4240675	0.90[CHB][hapmap]
rs4581006	0.95[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs4841529	0.81[JPT][hapmap]
rs4841530	0.90[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs4841537	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs4841539	0.85[CHB][hapmap];0.80[JPT][hapmap]
rs6601592	0.81[CHB][hapmap]
rs6982606	0.91[CHB][hapmap]
rs6984212	0.90[CHB][hapmap];0.81[JPT][hapmap];0.80[ASN][1000 genomes]
rs6998387	0.82[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7001675	0.95[CHB][hapmap]
rs7003814	0.85[CHB][hapmap]
rs7007712	0.90[CHB][hapmap]
rs7018402	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs7830445	0.85[ASN][1000 genomes]
rs7846252	0.90[CHB][hapmap];0.81[JPT][hapmap];0.83[ASN][1000 genomes]
rs9644687	0.95[CHB][hapmap];0.95[JPT][hapmap]
rs9693089	0.95[CHB][hapmap];0.88[ASN][1000 genomes]
rs9792166	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9792175	0.91[CHB][hapmap];0.80[JPT][hapmap]
rs9792227	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9792375	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs9792397	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 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	nsv1022525	chr8:11066191-11309356	Enhancers Genic enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv539474	chr8:11066191-11309356	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	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
7	nsv470183	chr8:11236975-11307118	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv465465	chr8:11245064-11307118	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv610275	chr8:11245064-11307118	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv522860	chr8:11253879-11330364	Bivalent/Poised TSS Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv890357	chr8:11286146-11330364	Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1030756	chr8:11292073-11332782	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	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

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs11782375	FAM167A	cis	Lymphoblastoid	GTEx
rs11782375	FAM167A	cis	Skin Sun Exposed Lower leg	GTEx
rs11782375	C8orf13	Cis_1M	lymphoblastoid	RTeQTL
rs11782375	BLK	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:11280600-11308800	Weak transcription	Primary B cells from cord blood	blood
2	chr8:11280800-11297600	Weak transcription	Spleen	Spleen
3	chr8:11286000-11295200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr8:11286200-11306400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr8:11286600-11296200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr8:11287400-11296400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:11287400-11296400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr8:11287400-11297600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr8:11287800-11300600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr8:11287800-11300600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr8:11287800-11313600	Weak transcription	Right Atrium	heart
12	chr8:11288000-11297600	Weak transcription	HSMM	muscle
13	chr8:11288200-11300200	Weak transcription	Brain Hippocampus Middle	brain
14	chr8:11289000-11295400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:11289000-11295600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:11289800-11299600	Weak transcription	Brain Anterior Caudate	brain
17	chr8:11289800-11305800	Weak transcription	Osteobl	bone
18	chr8:11291000-11295000	Enhancers	Fetal Thymus	thymus
19	chr8:11291200-11296200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:11291600-11296200	Weak transcription	Brain Cingulate Gyrus	brain
21	chr8:11291600-11303800	Weak transcription	Brain Angular Gyrus	brain
22	chr8:11291800-11300800	Weak transcription	NHEK	skin
23	chr8:11292000-11295200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr8:11292200-11296000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr8:11292400-11313000	Weak transcription	Pancreas	Pancrea
26	chr8:11292600-11295200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:11292600-11296400	Weak transcription	Thymus	Thymus
28	chr8:11292600-11302200	Weak transcription	Lung	lung
29	chr8:11292800-11297400	Weak transcription	Gastric	stomach
30	chr8:11293800-11297200	Weak transcription	Right Ventricle	heart
31	chr8:11294000-11295400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr8:11294000-11296400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr8:11294000-11297000	Weak transcription	Fetal Heart	heart
34	chr8:11294200-11296200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr8:11294400-11295400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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