Variant report

Variant	rs16926440
Chromosome Location	chr8:61644700-61644701
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10098584	1.00[ASN][1000 genomes]
rs10101023	1.00[ASN][1000 genomes]
rs13261519	1.00[ASN][1000 genomes]
rs13269361	1.00[ASN][1000 genomes]
rs13438807	1.00[ASN][1000 genomes]
rs16926379	1.00[ASN][1000 genomes]
rs16926398	1.00[ASN][1000 genomes]
rs16926444	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16926456	1.00[ASN][1000 genomes]
rs16926528	1.00[ASN][1000 genomes]
rs28539174	1.00[ASN][1000 genomes]
rs28539276	1.00[ASN][1000 genomes]
rs28667506	1.00[ASN][1000 genomes]
rs34833917	1.00[ASN][1000 genomes]
rs35777815	1.00[ASN][1000 genomes]
rs41272442	1.00[ASN][1000 genomes]
rs62524908	0.86[EUR][1000 genomes]
rs62524913	0.86[EUR][1000 genomes]
rs62524942	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524943	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524944	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524946	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524949	0.86[EUR][1000 genomes]
rs62524950	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524951	1.00[AFR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524952	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62524954	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62524956	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62524957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62526484	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs62526485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62526486	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs62526528	1.00[ASN][1000 genomes]
rs6471895	1.00[ASN][1000 genomes]
rs7013969	1.00[ASN][1000 genomes]
rs730084	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917756	chr8:60942299-61862796	Enhancers Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Active TSS 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	74 gene(s)	inside rSNPs	diseases
2	nsv831335	chr8:61497540-61688992	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS 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	33 gene(s)	inside rSNPs	diseases
3	nsv890945	chr8:61522008-61707725	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv526196	chr8:61593569-61877623	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv1022801	chr8:61623974-61738067	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv539632	chr8:61623974-61738067	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats 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	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61621200-61646400	Weak transcription	Fetal Brain Male	brain
2	chr8:61634800-61647000	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr8:61635000-61654200	Weak transcription	Fetal Intestine Small	intestine
4	chr8:61637000-61648600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:61637000-61648600	Weak transcription	HSMM	muscle
6	chr8:61637000-61651200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr8:61637000-61654600	Weak transcription	Hela-S3	cervix
8	chr8:61637800-61647600	Weak transcription	K562	blood
9	chr8:61638400-61645000	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr8:61638400-61648400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr8:61638600-61644800	Weak transcription	Lung	lung
12	chr8:61638600-61644800	Weak transcription	Pancreas	Pancrea
13	chr8:61638600-61648400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr8:61638600-61648400	Weak transcription	Gastric	stomach
15	chr8:61638600-61648400	Weak transcription	Stomach Mucosa	stomach
16	chr8:61638600-61648600	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr8:61638600-61651200	Weak transcription	Right Ventricle	heart
18	chr8:61638600-61654000	Weak transcription	NHEK	skin
19	chr8:61638600-61664200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr8:61639000-61644800	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr8:61639400-61644800	Weak transcription	Psoas Muscle	Psoas
22	chr8:61639400-61646800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr8:61639400-61647200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr8:61639400-61647800	Weak transcription	GM12878-XiMat	blood
25	chr8:61639400-61648400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr8:61640200-61644800	Weak transcription	Small Intestine	intestine
27	chr8:61641200-61646000	Weak transcription	Primary B cells from peripheral blood	blood
28	chr8:61642400-61649400	Enhancers	Primary neutrophils fromperipheralblood	blood
29	chr8:61643400-61645000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr8:61643400-61645200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr8:61643400-61646200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr8:61643400-61646400	Enhancers	HepG2	liver
33	chr8:61643600-61645200	Enhancers	Brain Substantia Nigra	brain
34	chr8:61643600-61645200	Enhancers	Left Ventricle	heart
35	chr8:61643600-61645400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr8:61643600-61646400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr8:61643800-61645000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
38	chr8:61643800-61645200	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr8:61644000-61644800	Enhancers	Primary T cells from cord blood	blood
40	chr8:61644000-61646200	Enhancers	Liver	Liver
41	chr8:61644200-61644800	Enhancers	Primary B cells from cord blood	blood
42	chr8:61644200-61644800	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr8:61644200-61645000	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr8:61644200-61645200	Enhancers	Brain Cingulate Gyrus	brain
45	chr8:61644200-61645200	Enhancers	Brain Germinal Matrix	brain
46	chr8:61644200-61645400	Enhancers	A549	lung
47	chr8:61644200-61646200	Enhancers	Brain Angular Gyrus	brain
48	chr8:61644200-61659200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr8:61644400-61644800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr8:61644400-61644800	Weak transcription	Duodenum Mucosa	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links