Variant report

Variant	rs9380505
Chromosome Location	chr6:35358764-35358765
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35358414..35360347-chr6:35370007..35371734,2	MCF-7	breast:
2	chr6:35357119..35359280-chr6:35381756..35383497,2	MCF-7	breast:
3	chr6:35313010..35315101-chr6:35358696..35360366,2	MCF-7	breast:
4	chr6:35337473..35339598-chr6:35358141..35360010,2	K562	blood:
5	chr6:35348461..35351306-chr6:35356739..35359433,2	MCF-7	breast:
6	chr6:35327015..35329027-chr6:35357004..35359462,2	K562	blood:
7	chr6:35352372..35354969-chr6:35356317..35359445,3	K562	blood:

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs12173347	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12173582	0.92[AFR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12211765	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1894652	0.89[EUR][1000 genomes]
rs1894653	0.89[EUR][1000 genomes]
rs2267660	0.89[EUR][1000 genomes]
rs2267661	0.89[EUR][1000 genomes]
rs2267664	0.92[AFR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3798342	0.89[EUR][1000 genomes]
rs3798343	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3800382	0.89[EUR][1000 genomes]
rs3800383	0.89[EUR][1000 genomes]
rs3800386	0.89[EUR][1000 genomes]
rs3800387	0.89[EUR][1000 genomes]
rs3800388	0.89[EUR][1000 genomes]
rs3800400	0.89[EUR][1000 genomes]
rs4583983	0.92[AFR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4711413	0.89[EUR][1000 genomes]
rs4713848	0.89[EUR][1000 genomes]
rs58925593	0.89[EUR][1000 genomes]
rs9296150	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9348974	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9366885	0.92[AFR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9368852	0.89[EUR][1000 genomes]
rs9368853	0.89[EUR][1000 genomes]
rs9368854	0.89[EUR][1000 genomes]
rs9368857	0.89[EUR][1000 genomes]
rs9368859	0.86[AFR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9368860	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9368865	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380502	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9380507	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9462072	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv830641	chr6:35282534-35440603	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	57 gene(s)	inside rSNPs	diseases
2	nsv462907	chr6:35333799-35408959	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv602908	chr6:35333799-35408959	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv602909	chr6:35356640-35423489	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35338400-35378400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr6:35338600-35359400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr6:35340600-35359400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr6:35345600-35378400	Weak transcription	Aorta	Aorta
5	chr6:35346200-35359200	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr6:35346200-35359800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr6:35347600-35359200	Weak transcription	Brain Angular Gyrus	brain
8	chr6:35347600-35359200	Weak transcription	Brain Substantia Nigra	brain
9	chr6:35349600-35359200	Weak transcription	Gastric	stomach
10	chr6:35350200-35359400	Weak transcription	Liver	Liver
11	chr6:35351000-35359000	Weak transcription	Primary T cells from cord blood	blood
12	chr6:35351000-35359200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:35351000-35359400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr6:35351000-35360200	Weak transcription	Primary B cells from peripheral blood	blood
15	chr6:35351000-35360800	Weak transcription	Primary B cells from cord blood	blood
16	chr6:35351000-35363400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:35351200-35359200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr6:35351200-35359400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr6:35351200-35359600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr6:35353800-35359000	Weak transcription	Brain Inferior Temporal Lobe	brain
21	chr6:35354000-35359000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr6:35354000-35359200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:35354000-35359200	Weak transcription	Brain Cingulate Gyrus	brain
24	chr6:35354000-35359200	Weak transcription	Fetal Lung	lung
25	chr6:35354000-35359200	Weak transcription	HSMMtube	muscle
26	chr6:35354000-35359400	Weak transcription	Left Ventricle	heart
27	chr6:35354000-35359600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr6:35354000-35359600	Weak transcription	Fetal Heart	heart
29	chr6:35354000-35359600	Weak transcription	Psoas Muscle	Psoas
30	chr6:35354000-35359800	Weak transcription	Fetal Stomach	stomach
31	chr6:35354000-35360800	Weak transcription	Fetal Thymus	thymus
32	chr6:35354000-35372400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr6:35354200-35359200	Weak transcription	NHDF-Ad	bronchial
34	chr6:35354400-35359800	Weak transcription	Rectal Smooth Muscle	rectum
35	chr6:35354600-35359200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr6:35354600-35359200	Weak transcription	Colon Smooth Muscle	Colon
37	chr6:35354800-35359200	Weak transcription	Brain Anterior Caudate	brain
38	chr6:35355000-35359400	Weak transcription	Right Ventricle	heart
39	chr6:35355000-35359600	Weak transcription	HepG2	liver
40	chr6:35355000-35359800	Weak transcription	Fetal Muscle Trunk	muscle
41	chr6:35355000-35364800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr6:35355200-35359200	Weak transcription	K562	blood
43	chr6:35355200-35359800	Weak transcription	Fetal Muscle Leg	muscle
44	chr6:35355400-35359000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:35356200-35359400	Weak transcription	Spleen	Spleen
46	chr6:35356200-35361000	Weak transcription	GM12878-XiMat	blood
47	chr6:35356400-35359200	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr6:35356400-35359400	Enhancers	Rectal Mucosa Donor 31	rectum
49	chr6:35356600-35359000	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr6:35356600-35359200	Weak transcription	Brain Hippocampus Middle	brain

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