Variant report

Variant	rs568536
Chromosome Location	chr17:67293580-67293581
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1011549	0.82[ASN][1000 genomes]
rs10445224	0.85[ASN][1000 genomes]
rs10512526	0.80[CHB][hapmap];0.95[JPT][hapmap]
rs10512527	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11077445	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs112914	1.00[JPT][hapmap]
rs11649744	0.82[ASN][1000 genomes]
rs11650955	0.90[CHB][hapmap];0.95[JPT][hapmap];0.81[ASN][1000 genomes]
rs11651815	0.89[ASN][1000 genomes]
rs11651872	0.89[ASN][1000 genomes]
rs11652207	0.95[JPT][hapmap];0.82[ASN][1000 genomes]
rs11654323	0.90[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs11656389	0.91[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs11656456	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs11869324	0.87[ASN][1000 genomes]
rs12449649	0.90[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12450167	0.90[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12450522	0.90[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs12450743	0.91[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs12452340	0.91[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs12937947	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs12938064	0.90[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs12938097	0.81[ASN][1000 genomes]
rs12940364	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs12941297	0.90[CHB][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs12942867	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs12943504	0.90[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12944980	0.82[ASN][1000 genomes]
rs12945481	0.91[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs12946566	0.88[ASN][1000 genomes]
rs12946776	0.83[ASN][1000 genomes]
rs12949267	0.96[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12952942	0.89[ASN][1000 genomes]
rs1468513	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs1550828	0.90[CHB][hapmap];0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs1558168	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs15886	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs1990248	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2364996	0.87[ASN][1000 genomes]
rs2441358	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34334829	0.88[ASN][1000 genomes]
rs34609440	0.88[ASN][1000 genomes]
rs34985085	0.82[ASN][1000 genomes]
rs4310935	0.89[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs4310936	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[ASN][1000 genomes]
rs471193	0.95[JPT][hapmap]
rs475283	0.95[JPT][hapmap]
rs476677	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs481876	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs486840	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs488714	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs494946	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs523505	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs531586	0.94[JPT][hapmap]
rs534645	1.00[JPT][hapmap]
rs544940	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs557491	0.90[CHB][hapmap];0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs55773491	0.89[ASN][1000 genomes]
rs57949169	0.86[ASN][1000 genomes]
rs6501313	1.00[JPT][hapmap]
rs7213377	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7223895	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7225762	0.80[CHB][hapmap];0.95[JPT][hapmap]
rs817121	1.00[JPT][hapmap]
rs817126	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs817127	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9646388	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv575932	chr17:67149973-67327806	Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer 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	15 gene(s)	inside rSNPs	diseases
2	nsv457889	chr17:67210992-67332355	Strong transcription Flanking Active TSS Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	n/a
3	nsv575934	chr17:67210992-67332355	ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	n/a
4	nsv833527	chr17:67240575-67400871	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv575935	chr17:67256162-67327806	ZNF genes & repeats Strong transcription Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	n/a
6	nsv457890	chr17:67264339-67327806	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	n/a
7	nsv575936	chr17:67264339-67327806	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	n/a
8	nsv1063768	chr17:67268342-67311136	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	n/a
9	esv1799828	chr17:67280310-67309039	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	n/a
10	nsv908706	chr17:67290840-67332355	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:67236800-67298800	Weak transcription	Psoas Muscle	Psoas
2	chr17:67240000-67296000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr17:67243600-67305600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr17:67244000-67321800	Weak transcription	Right Ventricle	heart
5	chr17:67261400-67322000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr17:67266200-67310400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr17:67268600-67295400	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr17:67270200-67307400	Weak transcription	Colonic Mucosa	Colon
9	chr17:67271000-67298600	Weak transcription	Fetal Lung	lung
10	chr17:67271400-67296000	Weak transcription	Fetal Kidney	kidney
11	chr17:67272400-67306400	Weak transcription	Primary B cells from peripheral blood	blood
12	chr17:67276400-67310600	Weak transcription	Brain Substantia Nigra	brain
13	chr17:67276600-67308800	Weak transcription	Aorta	Aorta
14	chr17:67277600-67293600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
15	chr17:67277800-67297000	Strong transcription	Rectal Mucosa Donor 31	rectum
16	chr17:67278200-67297600	Weak transcription	Brain Hippocampus Middle	brain
17	chr17:67279400-67308000	Weak transcription	Fetal Muscle Trunk	muscle
18	chr17:67279600-67306400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr17:67279800-67293600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr17:67280000-67307200	Weak transcription	Fetal Thymus	thymus
21	chr17:67283600-67297800	Weak transcription	Stomach Mucosa	stomach
22	chr17:67283600-67304800	Weak transcription	NHDF-Ad	bronchial
23	chr17:67283800-67312800	Weak transcription	HMEC	breast
24	chr17:67284000-67312800	Weak transcription	NHEK	skin
25	chr17:67284200-67301800	Weak transcription	Small Intestine	intestine
26	chr17:67284600-67309200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr17:67285000-67316200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr17:67286200-67297000	Weak transcription	Placenta	Placenta
29	chr17:67288200-67297200	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr17:67288400-67299200	Weak transcription	Fetal Intestine Small	intestine
31	chr17:67289600-67307000	Weak transcription	Spleen	Spleen
32	chr17:67289600-67307600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr17:67289600-67310400	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr17:67289800-67303200	Weak transcription	HUVEC	blood vessel
35	chr17:67289800-67310400	Weak transcription	Brain Anterior Caudate	brain
36	chr17:67289800-67310800	Weak transcription	Colon Smooth Muscle	Colon
37	chr17:67289800-67312800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr17:67290000-67294200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr17:67290000-67294600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr17:67290000-67295600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr17:67290000-67297600	Weak transcription	Fetal Muscle Leg	muscle
42	chr17:67290000-67299600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
43	chr17:67290000-67302400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
44	chr17:67290000-67305800	Weak transcription	Thymus	Thymus
45	chr17:67290000-67306200	Weak transcription	Primary T cells from cord blood	blood
46	chr17:67290000-67308200	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr17:67290000-67310600	Weak transcription	Brain Angular Gyrus	brain
48	chr17:67290000-67311000	Weak transcription	Primary hematopoietic stem cells	blood
49	chr17:67290000-67311000	Weak transcription	Rectal Smooth Muscle	rectum
50	chr17:67290000-67317400	Weak transcription	Gastric	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links