Variant report

Variant	rs9595827
Chromosome Location	chr13:48546575-48546576
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10220099	0.83[EUR][1000 genomes]
rs13378425	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2031775	0.83[EUR][1000 genomes]
rs2406701	0.98[EUR][1000 genomes]
rs28628659	0.83[EUR][1000 genomes]
rs28794608	0.98[EUR][1000 genomes]
rs4496017	0.97[EUR][1000 genomes]
rs55845516	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6561423	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7317676	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7319779	0.98[EUR][1000 genomes]
rs7983350	0.83[EUR][1000 genomes]
rs840431	0.97[EUR][1000 genomes]
rs840434	0.83[EUR][1000 genomes]
rs9316341	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9591118	0.83[EUR][1000 genomes]
rs9591119	0.83[EUR][1000 genomes]
rs9591120	0.83[EUR][1000 genomes]
rs9591121	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9591122	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9591124	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9591125	0.98[EUR][1000 genomes]
rs9591126	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9591128	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9595805	0.83[EUR][1000 genomes]
rs9595806	0.83[EUR][1000 genomes]
rs9595809	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9595810	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9595811	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9595814	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9595816	0.93[EUR][1000 genomes]
rs9595819	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9595826	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9595828	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9595830	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9595831	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9595832	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9595833	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933980	chr13:48431000-48557419	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
2	nsv430556	chr13:48516799-48679099	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 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	chr13:48507200-48548800	Weak transcription	Stomach Mucosa	stomach
2	chr13:48514400-48574000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr13:48532000-48551400	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr13:48532200-48565200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr13:48532400-48559400	Weak transcription	Gastric	stomach
6	chr13:48532400-48565200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr13:48533800-48548000	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr13:48534000-48560800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr13:48534200-48573200	Weak transcription	Brain Angular Gyrus	brain
10	chr13:48534400-48574400	Weak transcription	Small Intestine	intestine
11	chr13:48534600-48550400	Weak transcription	Right Ventricle	heart
12	chr13:48535000-48564800	Weak transcription	NHLF	lung
13	chr13:48535200-48552000	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr13:48536000-48550400	Weak transcription	Fetal Heart	heart
15	chr13:48536200-48550000	Weak transcription	NHEK	skin
16	chr13:48536800-48547800	Strong transcription	Liver	Liver
17	chr13:48537200-48574200	Weak transcription	Colonic Mucosa	Colon
18	chr13:48537400-48560200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr13:48537400-48574000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr13:48537400-48574400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:48538000-48567200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr13:48538400-48547200	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr13:48538400-48551000	Weak transcription	Fetal Brain Male	brain
24	chr13:48538400-48551600	Weak transcription	Brain Hippocampus Middle	brain
25	chr13:48538400-48574000	Weak transcription	Hela-S3	cervix
26	chr13:48538600-48559800	Weak transcription	HUVEC	blood vessel
27	chr13:48538800-48564800	Weak transcription	Brain Germinal Matrix	brain
28	chr13:48539400-48551800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr13:48539600-48571200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr13:48540000-48574200	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr13:48540200-48552600	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr13:48540200-48559000	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr13:48540600-48550000	Weak transcription	HSMMtube	muscle
34	chr13:48540800-48548400	Weak transcription	NHDF-Ad	bronchial
35	chr13:48540800-48565000	Weak transcription	NH-A	brain
36	chr13:48541200-48549200	Strong transcription	HUES64 Cell Line	embryonic stem cell
37	chr13:48541800-48550000	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr13:48542000-48548000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr13:48542000-48558800	Weak transcription	Sigmoid Colon	Sigmoid Colon
40	chr13:48542200-48546600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
41	chr13:48542400-48547400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr13:48542400-48551600	Weak transcription	HMEC	breast
43	chr13:48542400-48564800	Weak transcription	Rectal Smooth Muscle	rectum
44	chr13:48542400-48565200	Weak transcription	Psoas Muscle	Psoas
45	chr13:48542400-48567000	Weak transcription	Esophagus	oesophagus
46	chr13:48542600-48549800	Weak transcription	Ovary	ovary
47	chr13:48542800-48553800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr13:48542800-48559000	Weak transcription	HSMM	muscle
49	chr13:48543000-48553600	Weak transcription	Fetal Kidney	kidney
50	chr13:48543000-48574400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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