Variant report

Variant	rs1000457
Chromosome Location	chr17:33673428-33673429
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1081681	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11080339	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11080341	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11080342	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11080343	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12449840	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12451576	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12453983	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1399284	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1514490	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1533329	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1554043	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1554045	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1554046	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1949263	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1961017	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2376046	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2928997	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35716910	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3902986	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4074590	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4074591	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4503848	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4795071	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4796074	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6505458	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6505459	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6505461	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6505462	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7209244	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7211671	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7215259	0.87[CEU][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7219864	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7220501	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs772104	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8079268	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9893160	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9904880	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9915102	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1055936	chr17:33327166-33884184	Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
2	nsv543317	chr17:33327166-33884184	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
3	nsv534371	chr17:33456878-34094068	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv574741	chr17:33552275-33827134	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
5	nsv457724	chr17:33609247-33691409	Enhancers Weak transcription Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv574742	chr17:33609247-33691409	Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv457725	chr17:33664044-33774159	Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
8	nsv574743	chr17:33664044-33774159	Weak transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv515566	chr17:33664818-33768199	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh 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	11 gene(s)	inside rSNPs	diseases
10	nsv1066569	chr17:33671156-33758566	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1062610	chr17:33671466-33758566	Weak transcription Bivalent Enhancer Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:33672000-33674200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
2	chr17:33672200-33674200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr17:33672400-33673600	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
4	chr17:33672400-33673800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
5	chr17:33672400-33674000	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
6	chr17:33672400-33674000	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
7	chr17:33672400-33674000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
8	chr17:33672400-33674000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
9	chr17:33672400-33674000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
10	chr17:33672400-33674000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
11	chr17:33672400-33674000	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr17:33672400-33674000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
13	chr17:33672400-33674000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
14	chr17:33672400-33674000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
15	chr17:33672400-33674000	Active TSS	Right Atrium	heart
16	chr17:33672400-33674200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
17	chr17:33672400-33674200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
18	chr17:33672400-33674200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr17:33672400-33674200	Flanking Active TSS	Adipose Nuclei	Adipose
20	chr17:33672400-33674400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr17:33672600-33673800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr17:33672600-33673800	Flanking Active TSS	Primary hematopoietic stem cells	blood
23	chr17:33672600-33673800	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr17:33672600-33673800	Active TSS	Colon Smooth Muscle	Colon
25	chr17:33672600-33673800	Flanking Active TSS	Placenta	Placenta
26	chr17:33672600-33674000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
27	chr17:33672600-33674000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
28	chr17:33672600-33674000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
29	chr17:33672600-33674000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr17:33672600-33674000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr17:33672600-33674000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr17:33672600-33674000	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
33	chr17:33672600-33674000	Active TSS	Aorta	Aorta
34	chr17:33672600-33674000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
35	chr17:33672600-33674000	Active TSS	Right Ventricle	heart
36	chr17:33672600-33674000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
37	chr17:33672600-33674000	Flanking Active TSS	Dnd41	blood
38	chr17:33672800-33673600	Bivalent/Poised TSS	NH-A	brain
39	chr17:33672800-33673800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
40	chr17:33672800-33673800	Flanking Active TSS	Primary B cells from peripheral blood	blood
41	chr17:33672800-33673800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr17:33672800-33673800	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr17:33672800-33673800	Flanking Bivalent TSS/Enh	Fetal Thymus	thymus
44	chr17:33672800-33673800	Active TSS	Ovary	ovary
45	chr17:33672800-33673800	Active TSS	Placenta Amnion	Placenta Amnion
46	chr17:33672800-33674000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr17:33672800-33674000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr17:33672800-33674000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr17:33672800-33674000	Bivalent/Poised TSS	Brain Angular Gyrus	brain
50	chr17:33672800-33674000	Bivalent/Poised TSS	Colonic Mucosa	Colon

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links