Variant report

Variant	rs10758826
Chromosome Location	chr9:7105881-7105882
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs10122120	0.96[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10491781	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10491782	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1073496	0.93[CEU][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10758825	0.83[YRI][hapmap]
rs10758827	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10758828	1.00[CEU][hapmap];0.92[CHB][hapmap];0.91[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10758829	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10758830	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10758831	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10758832	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10815518	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10815519	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs10815520	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10976045	1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10976047	1.00[CHB][hapmap];0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10976052	0.96[CEU][hapmap];0.87[CHB][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12686272	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1323404	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1323405	1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1323406	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1323407	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1407863	0.82[YRI][hapmap]
rs1407867	0.85[CEU][hapmap]
rs2025324	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3763651	0.96[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3802400	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3802403	1.00[CHB][hapmap];0.85[JPT][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4740871	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs4740872	0.81[YRI][hapmap]
rs6477158	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6477159	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6477160	0.83[CEU][hapmap];1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs6477161	0.82[CEU][hapmap];1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs7021692	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7023759	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7023789	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7028048	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7037866	1.00[CEU][hapmap];0.94[CHB][hapmap];0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7042418	0.83[YRI][hapmap]
rs7048573	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7858101	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7860305	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7862227	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7862711	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7867958	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[YRI][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7869012	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7869317	0.92[CEU][hapmap];0.81[CHB][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7872366	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[YRI][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7872504	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7872625	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9299041	0.89[CEU][hapmap];0.93[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892166	chr9:6602821-7222495	Strong transcription Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
2	nsv1023906	chr9:6731786-7372132	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv613259	chr9:7032776-7541338	Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers 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	4 gene(s)	inside rSNPs	diseases
4	nsv1015874	chr9:7048807-7434890	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
5	nsv539971	chr9:7048807-7434890	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
6	nsv869932	chr9:7068359-7133384	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv892189	chr9:7091968-7150997	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv892190	chr9:7094860-7186074	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:7012200-7111200	Weak transcription	Colonic Mucosa	Colon
2	chr9:7088800-7128000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr9:7095400-7107400	Weak transcription	Fetal Kidney	kidney
4	chr9:7098600-7118000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr9:7098800-7108400	Weak transcription	HSMMtube	muscle
6	chr9:7099000-7106800	Weak transcription	Hela-S3	cervix
7	chr9:7100800-7120200	Strong transcription	Primary B cells from cord blood	blood
8	chr9:7102800-7114000	Strong transcription	Primary T cells from cord blood	blood
9	chr9:7103000-7106000	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr9:7103000-7110200	Strong transcription	Primary T helper cells fromperipheralblood	blood
11	chr9:7103000-7148600	Strong transcription	Primary B cells from peripheral blood	blood
12	chr9:7103200-7106000	Strong transcription	Primary T helper cells PMA-I stimulated	--
13	chr9:7103200-7108200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr9:7103200-7108200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr9:7103200-7116200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
16	chr9:7103400-7106200	Strong transcription	Duodenum Mucosa	Duodenum
17	chr9:7103400-7107200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:7103600-7106000	Strong transcription	Rectal Mucosa Donor 31	rectum
19	chr9:7103600-7106000	Strong transcription	Dnd41	blood
20	chr9:7103600-7106000	Strong transcription	K562	blood
21	chr9:7103600-7106200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr9:7103600-7106200	Strong transcription	Fetal Muscle Trunk	muscle
23	chr9:7103600-7106200	Strong transcription	GM12878-XiMat	blood
24	chr9:7103600-7118600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr9:7103800-7106000	Strong transcription	Adipose Nuclei	Adipose
26	chr9:7103800-7106000	Strong transcription	Rectal Mucosa Donor 29	rectum
27	chr9:7103800-7106400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr9:7103800-7128800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr9:7104000-7117800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr9:7104000-7121200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
31	chr9:7104200-7107000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr9:7104200-7117800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr9:7104200-7118000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr9:7104200-7118000	Weak transcription	HMEC	breast
35	chr9:7104200-7123600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr9:7104200-7128200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr9:7104200-7148200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr9:7104400-7106200	Weak transcription	A549	lung
39	chr9:7104400-7106200	Weak transcription	NHEK	skin
40	chr9:7104400-7107200	Weak transcription	Brain Angular Gyrus	brain
41	chr9:7104400-7113000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr9:7104400-7121200	Weak transcription	Esophagus	oesophagus
43	chr9:7104400-7121200	Weak transcription	Pancreas	Pancrea
44	chr9:7104400-7123600	Weak transcription	Gastric	stomach
45	chr9:7104400-7128000	Weak transcription	Aorta	Aorta
46	chr9:7104400-7128000	Weak transcription	Lung	lung
47	chr9:7104400-7135400	Weak transcription	Fetal Muscle Leg	muscle
48	chr9:7104400-7137600	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr9:7104400-7144600	Weak transcription	Brain Anterior Caudate	brain
50	chr9:7104600-7148000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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