Variant report

Variant	rs9658083
Chromosome Location	chr6:35337291-35337292
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:35335918..35340012-chr6:35342665..35344421,4	K562	blood:
2	chr6:35335380..35337947-chr6:35338128..35341057,2	MCF-7	breast:
3	chr6:35337130..35339523-chr6:35342584..35344904,3	MCF-7	breast:
4	chr6:35335918..35339865-chr6:35340596..35344421,5	K562	blood:
5	chr6:35329439..35333357-chr6:35335770..35342563,9	K562	blood:
6	chr6:35319838..35321444-chr6:35336659..35338777,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1053046	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11571504	0.96[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13362808	0.82[ASN][1000 genomes]
rs3213573	1.00[JPT][hapmap]
rs57648364	0.82[ASN][1000 genomes]
rs59137976	0.82[ASN][1000 genomes]
rs6457813	1.00[JPT][hapmap]
rs6457816	0.88[CEU][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6900530	1.00[JPT][hapmap]
rs6901410	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6902123	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6906237	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6919334	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6922548	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6937088	0.91[ASN][1000 genomes]
rs6942357	0.96[ASN][1000 genomes]
rs707969	1.00[JPT][hapmap]
rs73413718	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7739752	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7746988	1.00[JPT][hapmap]
rs7754871	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9296148	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9296154	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9470001	1.00[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9470007	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9470016	0.82[ASN][1000 genomes]
rs9658067	0.82[ASN][1000 genomes]
rs9658100	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9658125	1.00[JPT][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 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

No data

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35321000-35342400	Weak transcription	Fetal Kidney	kidney
2	chr6:35328400-35344800	Weak transcription	Fetal Lung	lung
3	chr6:35329000-35350800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:35329200-35337800	Weak transcription	Ovary	ovary
5	chr6:35329600-35338400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr6:35331200-35337800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:35331200-35350800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr6:35331400-35337600	Weak transcription	Colonic Mucosa	Colon
9	chr6:35331400-35337800	Weak transcription	Aorta	Aorta
10	chr6:35331400-35337800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr6:35331400-35339200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr6:35331600-35337800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:35331600-35337800	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chr6:35331600-35338000	Weak transcription	Gastric	stomach
15	chr6:35331600-35345400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:35331600-35345400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:35332000-35337800	Weak transcription	Brain Anterior Caudate	brain
18	chr6:35332200-35338000	Weak transcription	Brain Angular Gyrus	brain
19	chr6:35334200-35339800	Enhancers	K562	blood
20	chr6:35334800-35339400	Enhancers	Psoas Muscle	Psoas
21	chr6:35335000-35337600	Enhancers	HSMMtube	muscle
22	chr6:35335000-35337800	Enhancers	Skeletal Muscle Male	skeletal muscle
23	chr6:35335000-35339800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:35335200-35337800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr6:35335200-35337800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr6:35335400-35337400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:35335400-35337800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr6:35335400-35337800	Enhancers	NH-A	brain
29	chr6:35335400-35338600	Enhancers	HepG2	liver
30	chr6:35335400-35339400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:35335400-35339800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
32	chr6:35335400-35339800	Enhancers	Adipose Nuclei	Adipose
33	chr6:35335400-35340000	Enhancers	Primary T cells fromperipheralblood	blood
34	chr6:35335600-35337600	Enhancers	Muscle Satellite Cultured Cells	--
35	chr6:35335600-35337600	Enhancers	Rectal Mucosa Donor 29	rectum
36	chr6:35335600-35337800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr6:35335600-35337800	Enhancers	NHDF-Ad	bronchial
38	chr6:35335600-35337800	Enhancers	NHEK	skin
39	chr6:35335600-35338200	Weak transcription	Fetal Stomach	stomach
40	chr6:35335600-35338800	Enhancers	Breast Myoepithelial Primary Cells	Breast
41	chr6:35335600-35339000	Enhancers	Hela-S3	cervix
42	chr6:35335600-35339200	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr6:35335600-35339400	Enhancers	Small Intestine	intestine
44	chr6:35335600-35339400	Enhancers	Dnd41	blood
45	chr6:35335600-35339800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
46	chr6:35335800-35337800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr6:35335800-35337800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
48	chr6:35335800-35338000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:35335800-35338000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr6:35335800-35339600	Enhancers	Sigmoid Colon	Sigmoid Colon

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