Variant report

Variant	rs7847658
Chromosome Location	chr9:7012574-7012575
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10815506	0.93[ASN][1000 genomes]
rs10975956	0.87[ASN][1000 genomes]
rs10975961	0.93[ASN][1000 genomes]
rs10975987	0.90[EUR][1000 genomes]
rs12236552	0.90[EUR][1000 genomes]
rs2381533	0.93[EUR][1000 genomes]
rs35389625	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4742284	0.93[EUR][1000 genomes]
rs58212305	1.00[AFR][1000 genomes]
rs59494877	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7466171	0.93[EUR][1000 genomes]
rs7854837	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs818884	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv870402	chr9:6565246-7016784	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
2	nsv1033539	chr9:6566610-7022554	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
3	nsv466111	chr9:6567841-7017391	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	nsv613208	chr9:6567841-7017391	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv1024831	chr9:6573752-7018641	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
6	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
7	nsv892181	chr9:6680477-7070962	Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	70 gene(s)	inside rSNPs	diseases
8	nsv613252	chr9:6715730-7022554	Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	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
10	nsv1023461	chr9:6774993-7022554	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
11	nsv831501	chr9:6868099-7058526	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	nsv892185	chr9:6929053-7070962	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	nsv1021234	chr9:6933222-7015397	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	nsv870178	chr9:6941584-7060029	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv892186	chr9:6942605-7075305	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv892187	chr9:6974101-7035727	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
17	nsv949711	chr9:6994399-7045058	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
18	nsv892188	chr9:6999846-7026860	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:6972000-7013200	Weak transcription	Fetal Kidney	kidney
2	chr9:6979800-7018600	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr9:6984000-7018200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr9:6985600-7019200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr9:6985600-7035600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr9:6986800-7015600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr9:7003400-7012800	Weak transcription	Brain Germinal Matrix	brain
8	chr9:7007800-7019000	Strong transcription	Rectal Mucosa Donor 29	rectum
9	chr9:7008000-7014200	Strong transcription	Adipose Nuclei	Adipose
10	chr9:7008000-7018800	Strong transcription	Duodenum Mucosa	Duodenum
11	chr9:7008000-7018800	Strong transcription	Sigmoid Colon	Sigmoid Colon
12	chr9:7008200-7014200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr9:7008200-7014800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr9:7008600-7016000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:7008800-7017000	Weak transcription	NHLF	lung
16	chr9:7008800-7024200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr9:7009000-7015800	Weak transcription	Gastric	stomach
18	chr9:7009000-7017400	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr9:7009000-7018000	Weak transcription	Lung	lung
20	chr9:7009000-7019000	Strong transcription	Monocytes-CD14+_RO01746	blood
21	chr9:7009000-7019800	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr9:7009000-7021600	Weak transcription	HMEC	breast
23	chr9:7009000-7026200	Weak transcription	A549	lung
24	chr9:7009000-7027400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
25	chr9:7009000-7027800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr9:7009000-7027800	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr9:7009000-7028400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr9:7009000-7030400	Weak transcription	NHEK	skin
29	chr9:7009000-7044800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:7009000-7046200	Weak transcription	Small Intestine	intestine
31	chr9:7009000-7055200	Weak transcription	K562	blood
32	chr9:7009000-7056400	Weak transcription	Brain Substantia Nigra	brain
33	chr9:7009000-7076600	Weak transcription	HSMM	muscle
34	chr9:7009200-7016400	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr9:7009200-7017400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr9:7009200-7077600	Weak transcription	Osteobl	bone
37	chr9:7009400-7016400	Weak transcription	Brain Hippocampus Middle	brain
38	chr9:7009400-7016800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
39	chr9:7009400-7019200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
40	chr9:7009400-7029600	Weak transcription	Hela-S3	cervix
41	chr9:7009400-7042000	Weak transcription	NHDF-Ad	bronchial
42	chr9:7009600-7020400	Strong transcription	Primary B cells from cord blood	blood
43	chr9:7009800-7018000	Weak transcription	Fetal Brain Female	brain
44	chr9:7009800-7076600	Weak transcription	HSMMtube	muscle
45	chr9:7010400-7013200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr9:7010400-7020600	Strong transcription	Primary B cells from peripheral blood	blood
47	chr9:7010600-7016200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr9:7011000-7021000	Strong transcription	Primary T helper cells PMA-I stimulated	--
49	chr9:7011200-7019600	Strong transcription	Liver	Liver
50	chr9:7011400-7012800	Strong transcription	Brain Inferior Temporal Lobe	brain

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