Variant report

Variant	rs9747574
Chromosome Location	chr17:37626516-37626517
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs12940109	1.00[AMR][1000 genomes]
rs12940881	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12940956	1.00[AMR][1000 genomes]
rs12945363	1.00[AMR][1000 genomes]
rs12947238	1.00[AMR][1000 genomes]
rs12953178	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34821956	1.00[AMR][1000 genomes]
rs34904106	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34910003	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs34983824	1.00[AMR][1000 genomes]
rs35194764	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35269184	1.00[AMR][1000 genomes]
rs35366897	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35499078	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35656573	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35829705	1.00[AMR][1000 genomes]
rs35853230	1.00[AMR][1000 genomes]
rs35896550	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57938769	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59775294	1.00[AMR][1000 genomes]
rs6503512	1.00[AMR][1000 genomes]
rs71369747	0.83[AMR][1000 genomes]
rs71369760	0.83[AMR][1000 genomes]
rs71369763	1.00[AMR][1000 genomes]
rs71369765	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71369767	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs71577045	0.83[AMR][1000 genomes]
rs7212530	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7212780	1.00[AMR][1000 genomes]
rs7218668	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7226222	1.00[AMR][1000 genomes]
rs8064372	1.00[AMR][1000 genomes]
rs8069194	1.00[AMR][1000 genomes]
rs8073144	1.00[AMR][1000 genomes]
rs8074199	1.00[AMR][1000 genomes]
rs8076843	1.00[AMR][1000 genomes]
rs8077259	1.00[AMR][1000 genomes]
rs8077822	1.00[AMR][1000 genomes]
rs8079346	1.00[AMR][1000 genomes]
rs8080830	1.00[AMR][1000 genomes]
rs8081561	1.00[AMR][1000 genomes]
rs9747666	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	nsv1060126	chr17:37333956-37659189	Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv1057655	chr17:37333956-37732451	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
4	nsv1066033	chr17:37333956-37795617	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
5	nsv543340	chr17:37333956-37795617	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	78 gene(s)	inside rSNPs	diseases
6	nsv908204	chr17:37349655-37682657	Genic enhancers Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
7	nsv1057057	chr17:37395082-37627025	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv1061951	chr17:37442228-37770903	Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv543341	chr17:37442228-37770903	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
10	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
11	nsv532712	chr17:37521822-37768345	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
12	nsv1063848	chr17:37575622-37707592	Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37619600-37627200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr17:37619800-37627200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:37619800-37649200	Weak transcription	Esophagus	oesophagus
4	chr17:37620200-37627200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr17:37620400-37627400	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr17:37620400-37650600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr17:37620800-37626800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr17:37620800-37627200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr17:37621000-37626600	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr17:37621000-37626800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
11	chr17:37621000-37627000	Weak transcription	HSMMtube	muscle
12	chr17:37621000-37627200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr17:37621000-37627200	Weak transcription	Right Ventricle	heart
14	chr17:37621000-37627600	Weak transcription	Colonic Mucosa	Colon
15	chr17:37621200-37626800	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr17:37621200-37626800	Weak transcription	Colon Smooth Muscle	Colon
17	chr17:37621200-37626800	Weak transcription	HMEC	breast
18	chr17:37621200-37627000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr17:37621200-37627000	Weak transcription	Brain Substantia Nigra	brain
20	chr17:37621200-37627200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr17:37621200-37627200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr17:37621200-37627200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr17:37621200-37627200	Weak transcription	Aorta	Aorta
24	chr17:37621200-37627200	Weak transcription	Gastric	stomach
25	chr17:37621200-37627200	Weak transcription	Psoas Muscle	Psoas
26	chr17:37621400-37630400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr17:37621600-37626800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr17:37621600-37627200	Weak transcription	Thymus	Thymus
29	chr17:37621800-37626800	Weak transcription	Primary hematopoietic stem cells	blood
30	chr17:37621800-37626800	Weak transcription	NH-A	brain
31	chr17:37621800-37626800	Weak transcription	NHEK	skin
32	chr17:37621800-37627000	Weak transcription	NHLF	lung
33	chr17:37622000-37627000	Weak transcription	Fetal Muscle Trunk	muscle
34	chr17:37622000-37627000	Weak transcription	Left Ventricle	heart
35	chr17:37622000-37627200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr17:37622000-37627200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr17:37622000-37627200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr17:37622000-37627200	Weak transcription	Lung	lung
39	chr17:37622000-37627200	Weak transcription	Ovary	ovary
40	chr17:37622000-37627200	Weak transcription	Pancreas	Pancrea
41	chr17:37622000-37627200	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr17:37622000-37627200	Weak transcription	Small Intestine	intestine
43	chr17:37622000-37627200	Weak transcription	Stomach Smooth Muscle	stomach
44	chr17:37622200-37626600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr17:37622200-37626600	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr17:37622200-37626800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
47	chr17:37622200-37627000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr17:37622200-37627000	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr17:37622200-37627200	Weak transcription	Brain Cingulate Gyrus	brain
50	chr17:37622200-37633400	Strong transcription	Primary B cells from peripheral blood	blood

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