Variant report

Variant	rs9446260
Chromosome Location	chr6:71245978-71245979
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10080714	0.84[AFR][1000 genomes]
rs10440813	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10485117	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs12332812	0.91[YRI][hapmap];0.84[AFR][1000 genomes]
rs12332923	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16869217	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16869242	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16869261	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16869301	0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2207424	0.93[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2223997	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28555262	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28885692	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3846749	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs747454	0.93[YRI][hapmap];0.84[AFR][1000 genomes]
rs9294867	0.91[YRI][hapmap];0.81[AFR][1000 genomes]
rs9294869	0.93[YRI][hapmap];0.84[AFR][1000 genomes]
rs9294870	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs9294873	0.93[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9294875	0.81[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9294877	0.81[AFR][1000 genomes]
rs9446243	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs9446244	0.83[YRI][hapmap]
rs9446247	0.93[YRI][hapmap];0.84[AFR][1000 genomes]
rs9446251	0.93[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446253	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446255	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446256	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446257	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446259	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446261	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446262	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446263	0.98[AFR][1000 genomes]
rs9446264	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446265	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9446266	0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455091	0.91[YRI][hapmap]
rs9455096	1.00[YRI][hapmap]
rs9455102	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs9455103	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs9455107	0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455109	0.92[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455110	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455112	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455115	0.82[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455116	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455117	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455118	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455119	0.82[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455120	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455122	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455123	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455124	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455126	0.91[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455127	0.85[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455128	0.93[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455131	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455134	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455135	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455136	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455137	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455141	0.92[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455142	0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455143	0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455145	0.92[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455146	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455147	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455148	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455152	0.91[YRI][hapmap];0.93[AFR][1000 genomes]
rs9455154	0.93[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455155	0.91[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455157	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455159	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9455183	0.81[AFR][1000 genomes]
rs9455184	0.81[AFR][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	nsv932111	chr6:70736835-71633094	Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer 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	31 gene(s)	inside rSNPs	diseases
2	nsv886142	chr6:70741209-71251421	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv1027049	chr6:70961610-71561488	Strong transcription Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv524328	chr6:70961833-71558805	Flanking Bivalent TSS/Enh Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
5	nsv917312	chr6:70961903-71601688	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
6	nsv886145	chr6:71119524-71317480	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
7	nsv886146	chr6:71219464-71317480	Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71210600-71262000	Weak transcription	Fetal Thymus	thymus
2	chr6:71214000-71248600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:71214000-71248800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr6:71214000-71249600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr6:71214000-71250600	Weak transcription	Right Ventricle	heart
6	chr6:71214000-71253000	Weak transcription	Colonic Mucosa	Colon
7	chr6:71214000-71253000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr6:71214000-71256600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:71214000-71276000	Weak transcription	Brain Angular Gyrus	brain
10	chr6:71214000-71276000	Weak transcription	Brain Germinal Matrix	brain
11	chr6:71214000-71276000	Weak transcription	Colon Smooth Muscle	Colon
12	chr6:71214200-71248200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:71214400-71246000	Weak transcription	HMEC	breast
14	chr6:71214400-71251000	Weak transcription	Brain Substantia Nigra	brain
15	chr6:71214400-71251800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr6:71214400-71257000	Weak transcription	Brain Anterior Caudate	brain
17	chr6:71214400-71262000	Weak transcription	Psoas Muscle	Psoas
18	chr6:71214600-71248200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr6:71214600-71248600	Weak transcription	NHEK	skin
20	chr6:71214600-71248800	Weak transcription	Brain Hippocampus Middle	brain
21	chr6:71214600-71251200	Weak transcription	K562	blood
22	chr6:71214600-71276000	Weak transcription	A549	lung
23	chr6:71215000-71273000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr6:71216200-71262200	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr6:71219000-71258800	Weak transcription	Small Intestine	intestine
26	chr6:71225200-71248800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:71228000-71248800	Weak transcription	Fetal Kidney	kidney
28	chr6:71228600-71276000	Weak transcription	Primary T cells from cord blood	blood
29	chr6:71229600-71276200	Weak transcription	Aorta	Aorta
30	chr6:71229800-71248800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr6:71230400-71247400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:71231200-71268000	Weak transcription	Brain Cingulate Gyrus	brain
33	chr6:71231800-71257200	Weak transcription	Fetal Heart	heart
34	chr6:71232800-71251200	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr6:71233400-71248800	Weak transcription	Fetal Brain Female	brain
36	chr6:71233400-71256800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr6:71234800-71250800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr6:71234800-71256600	Weak transcription	HepG2	liver
39	chr6:71235600-71258200	Weak transcription	Liver	Liver
40	chr6:71236000-71246800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr6:71236400-71248800	Weak transcription	Fetal Lung	lung
42	chr6:71236400-71273200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:71237000-71248200	Weak transcription	Rectal Mucosa Donor 29	rectum
44	chr6:71237000-71276200	Weak transcription	Left Ventricle	heart
45	chr6:71237600-71248400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
46	chr6:71237600-71257400	Weak transcription	Osteobl	bone
47	chr6:71240200-71251600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr6:71240600-71254000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr6:71240800-71253800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:71240800-71256400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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