Variant report

Variant	rs8066902
Chromosome Location	chr17:15882922-15882923
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15873717..15876344-chr17:15882038..15883572,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 21 )

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1045599	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11654	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11655456	0.81[EUR][1000 genomes]
rs11869450	0.80[EUR][1000 genomes]
rs11869563	0.81[EUR][1000 genomes]
rs1860643	0.86[AMR][1000 genomes]
rs1860644	0.82[AMR][1000 genomes]
rs1860645	0.84[AMR][1000 genomes]
rs2015353	0.80[AMR][1000 genomes]
rs2109632	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2159643	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2286795	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2286796	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2535614	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2779207	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2779208	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2779210	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs2779212	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3760297	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4792707	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4792708	0.80[EUR][1000 genomes]
rs4792709	0.81[EUR][1000 genomes]
rs4792712	0.81[EUR][1000 genomes]
rs4792713	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4792715	0.80[EUR][1000 genomes]
rs6416868	0.80[EUR][1000 genomes]
rs6502482	0.80[AMR][1000 genomes]
rs7209094	0.81[EUR][1000 genomes]
rs7210655	0.81[EUR][1000 genomes]
rs7216949	0.81[EUR][1000 genomes]
rs8070859	0.81[EUR][1000 genomes]
rs9891938	0.82[AMR][1000 genomes]
rs9897542	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	nsv1062951	chr17:15561070-15890644	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
5	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
6	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
7	nsv907706	chr17:15731923-16056442	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
8	nsv1067555	chr17:15804228-16001117	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
9	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	164 gene(s)	inside rSNPs	diseases
10	nsv907707	chr17:15846535-15950751	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	nsv907709	chr17:15851196-15937487	Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
12	nsv907708	chr17:15851196-15950751	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
13	nsv1057493	chr17:15852125-15930718	Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv543215	chr17:15852125-15930718	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats 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
15	nsv907710	chr17:15854257-15950751	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
16	nsv1062220	chr17:15869557-16093156	Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
17	nsv1064878	chr17:15869557-16097241	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
18	nsv1055173	chr17:15875935-16097241	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
19	esv1788130	chr17:15882921-15883179	Weak transcription Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:21)

SNP	Gene	Cis/trans	Tissue	Source
rs8066902	LOC100131909	cis	intralobular white matter	BrainEAC
rs8066902	LOC100131909	cis	frontal cortex	BrainEAC
rs8066902	LOC100131909	cis	cerebellar cortex	BrainEAC
rs8066902	LOC100131909	cis	inferior olivary nucleus	BrainEAC
rs8066902	ADORA2B	cis	Muscle Skeletal	GTEx
rs8066902	LOC100131909	cis	occipital cortex	BrainEAC
rs8066902	ADORA2B	cis	Thyroid	GTEx
rs8066902	LOC100131909	cis	brain	BrainEAC
rs8066902	ADORA2B	cis	Esophagus Muscularis	GTEx
rs8066902	ZSWIM7	cis	Muscle Skeletal	GTEx
rs8066902	LOC100131909	cis	thalamus	BrainEAC
rs8066902	ADORA2B	cis	Nerve Tibial	GTEx
rs8066902	ADORA2B	cis	Artery Tibial	GTEx
rs8066902	LOC100131909	cis	temporal cortex	BrainEAC
rs8066902	ADORA2B	cis	Adipose Subcutaneous	GTEx
rs8066902	TTC19	Cis_1M	lymphoblastoid	RTeQTL
rs8066902	ZSWIM7	Cis_1M	lymphoblastoid	RTeQTL
rs8066902	ADORA2B	cis	lung	GTEx
rs8066902	LOC100131909	cis	substantia nigra	BrainEAC
rs8066902	LOC100131909	cis	putamen	BrainEAC
rs8066902	LOC100131909	cis	hippocampus	BrainEAC

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15870200-15883600	Weak transcription	Fetal Heart	heart
2	chr17:15870400-15883600	Weak transcription	Brain Angular Gyrus	brain
3	chr17:15870400-15883800	Weak transcription	Gastric	stomach
4	chr17:15870400-15902400	Weak transcription	Small Intestine	intestine
5	chr17:15870600-15883600	Weak transcription	Pancreas	Pancrea
6	chr17:15870600-15883800	Weak transcription	Fetal Brain Male	brain
7	chr17:15870800-15902400	Weak transcription	Esophagus	oesophagus
8	chr17:15872000-15883400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr17:15873200-15902200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr17:15874600-15883600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr17:15874800-15902400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr17:15875200-15884200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
13	chr17:15876600-15885400	Weak transcription	Hela-S3	cervix
14	chr17:15877600-15883600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr17:15877600-15888800	Weak transcription	NHDF-Ad	bronchial
16	chr17:15877800-15891200	Strong transcription	Fetal Muscle Leg	muscle
17	chr17:15878200-15901800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr17:15878400-15883800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr17:15878800-15883800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr17:15878800-15883800	Weak transcription	NHLF	lung
21	chr17:15879000-15884600	Weak transcription	NH-A	brain
22	chr17:15879600-15891600	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr17:15880000-15883600	Strong transcription	H1 Cell Line	embryonic stem cell
24	chr17:15880200-15901600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr17:15880600-15883800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
26	chr17:15880800-15883400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr17:15880800-15883600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr17:15880800-15883600	Weak transcription	Right Ventricle	heart
29	chr17:15880800-15883800	Weak transcription	Psoas Muscle	Psoas
30	chr17:15881200-15883600	Weak transcription	Primary B cells from peripheral blood	blood
31	chr17:15881200-15892800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr17:15881400-15883600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr17:15881400-15901800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
34	chr17:15881600-15883600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr17:15881600-15883600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr17:15881600-15883600	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr17:15881600-15883600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr17:15881600-15883600	Weak transcription	Fetal Thymus	thymus
39	chr17:15881600-15883600	Weak transcription	A549	lung
40	chr17:15881600-15883600	Weak transcription	Dnd41	blood
41	chr17:15881600-15883800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr17:15881600-15885400	Weak transcription	Primary neutrophils fromperipheralblood	blood
43	chr17:15881800-15883400	Weak transcription	Brain Germinal Matrix	brain
44	chr17:15881800-15883600	Weak transcription	H9 Cell Line	embryonic stem cell
45	chr17:15881800-15883600	Weak transcription	Colon Smooth Muscle	Colon
46	chr17:15881800-15883800	Weak transcription	Colonic Mucosa	Colon
47	chr17:15881800-15888000	Weak transcription	HepG2	liver
48	chr17:15882000-15883400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr17:15882000-15883400	Weak transcription	Fetal Stomach	stomach
50	chr17:15882000-15884200	Weak transcription	Fetal Intestine Small	intestine

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