Variant report

Variant	rs7934817
Chromosome Location	chr11:18538040-18538041
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	chr11:18533757..18535476-chr11:18537479..18539659,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10500836	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10741747	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10766483	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10766484	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10766485	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10832940	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11024690	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11024699	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11024711	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12224694	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12225037	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12419063	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12574808	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12577346	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1395319	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1395320	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34457574	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3925781	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4298881	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4623881	0.85[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4756949	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4756950	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4756952	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs56333121	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6486434	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7105889	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7107057	0.90[AFR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7928872	0.80[AMR][1000 genomes]
rs7931630	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7951508	0.89[AFR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7952284	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs868069	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[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	nsv949248	chr11:17791822-18692687	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	156 gene(s)	inside rSNPs	diseases
2	nsv553633	chr11:18311701-19058451	Weak transcription Strong transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
3	nsv1038015	chr11:18435855-18558211	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
4	nsv1042155	chr11:18435855-18697576	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
5	nsv467719	chr11:18447611-18542227	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv553634	chr11:18447611-18542227	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
7	nsv820064	chr11:18537683-18538721	Strong transcription Weak transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7934817	TSG101	cis	Esophagus Mucosa	GTEx
rs7934817	LDHC	cis	Thyroid	GTEx
rs7934817	TSG101	Cis_1M	lymphoblastoid	RTeQTL
rs7934817	TSG101	cis	Muscle Skeletal	GTEx

Chromatin state (count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:18496200-18541200	Strong transcription	Monocytes-CD14+_RO01746	blood
2	chr11:18496400-18542000	Strong transcription	Primary T cells fromperipheralblood	blood
3	chr11:18496600-18540600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr11:18496600-18541000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
5	chr11:18500000-18547000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:18504000-18540600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr11:18509000-18540200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:18509000-18540600	Strong transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:18509600-18540200	Strong transcription	Placenta	Placenta
10	chr11:18510800-18541400	Strong transcription	Primary B cells from peripheral blood	blood
11	chr11:18513000-18544000	Weak transcription	Gastric	stomach
12	chr11:18513000-18544000	Weak transcription	Psoas Muscle	Psoas
13	chr11:18513000-18547600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr11:18514600-18540800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr11:18514800-18539800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr11:18515000-18540000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr11:18515000-18540600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:18515400-18547200	Weak transcription	Stomach Mucosa	stomach
19	chr11:18516200-18538200	Strong transcription	Adipose Nuclei	Adipose
20	chr11:18516200-18538800	Strong transcription	Fetal Muscle Trunk	muscle
21	chr11:18516200-18540400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr11:18516400-18540400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr11:18516800-18541800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:18517200-18540400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr11:18518000-18539200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
26	chr11:18518200-18538600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr11:18518200-18540400	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr11:18519200-18540600	Strong transcription	Duodenum Mucosa	Duodenum
29	chr11:18519200-18540800	Strong transcription	HUES48 Cell Line	embryonic stem cell
30	chr11:18519200-18540800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr11:18519400-18540400	Strong transcription	Primary T cells from cord blood	blood
32	chr11:18521400-18540800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr11:18523800-18547400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr11:18524200-18547200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr11:18524200-18547400	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr11:18525600-18538200	Strong transcription	Duodenum Smooth Muscle	Duodenum
37	chr11:18525800-18540000	Strong transcription	HUES64 Cell Line	embryonic stem cell
38	chr11:18526000-18540800	Strong transcription	Fetal Brain Female	brain
39	chr11:18527200-18547200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr11:18527600-18545400	Weak transcription	Small Intestine	intestine
41	chr11:18530200-18539200	Strong transcription	Fetal Lung	lung
42	chr11:18530200-18540400	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr11:18531200-18540600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
44	chr11:18531200-18544600	Weak transcription	Hela-S3	cervix
45	chr11:18531400-18546600	Weak transcription	K562	blood
46	chr11:18532200-18540400	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr11:18532600-18540200	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:18532800-18547400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr11:18533200-18540000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr11:18533400-18547200	Weak transcription	A549	lung

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