Variant report

Variant	rs13133491
Chromosome Location	chr4:110424735-110424736
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10016533	0.90[EUR][1000 genomes]
rs10025781	0.87[EUR][1000 genomes]
rs10452150	0.93[EUR][1000 genomes]
rs13110999	0.93[EUR][1000 genomes]
rs13122093	0.93[EUR][1000 genomes]
rs13132816	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13140373	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13147210	0.80[EUR][1000 genomes]
rs13151464	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs13151516	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs15821	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs33911248	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs34132975	0.93[EUR][1000 genomes]
rs34133579	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34320670	0.84[EUR][1000 genomes]
rs34368920	0.85[EUR][1000 genomes]
rs34473874	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs34502105	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34660885	0.93[EUR][1000 genomes]
rs34710885	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34727629	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34813537	0.93[EUR][1000 genomes]
rs34851707	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34861128	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs34953524	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35199349	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35313553	0.93[EUR][1000 genomes]
rs35329136	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35450490	0.93[EUR][1000 genomes]
rs35598950	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35699695	0.93[EUR][1000 genomes]
rs35865655	0.87[EUR][1000 genomes]
rs35866656	0.93[EUR][1000 genomes]
rs35950484	0.93[EUR][1000 genomes]
rs36102563	0.93[EUR][1000 genomes]
rs41277037	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6533434	0.85[EUR][1000 genomes]
rs66493839	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67066117	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67727505	0.89[EUR][1000 genomes]
rs67923759	0.93[EUR][1000 genomes]
rs6828719	0.87[EUR][1000 genomes]
rs6834685	0.85[EUR][1000 genomes]
rs71603034	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs71603035	0.87[EUR][1000 genomes]
rs72672698	0.87[EUR][1000 genomes]
rs7694710	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv461613	chr4:109922064-110593460	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv595129	chr4:109922064-110593460	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	esv3349784	chr4:110348873-110723163	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers 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	35 gene(s)	inside rSNPs	diseases
4	nsv525385	chr4:110395146-110466413	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region miRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:110393800-110469200	Weak transcription	Stomach Mucosa	stomach
2	chr4:110400200-110455400	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr4:110402000-110425000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:110409400-110467800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr4:110411400-110464600	Strong transcription	Primary monocytes fromperipheralblood	blood
6	chr4:110412400-110425400	Strong transcription	Primary T cells from cord blood	blood
7	chr4:110412400-110430200	Strong transcription	Liver	Liver
8	chr4:110412400-110443000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr4:110412400-110444600	Strong transcription	Primary T cells fromperipheralblood	blood
10	chr4:110412400-110465400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr4:110412400-110466200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:110412400-110470600	Strong transcription	Fetal Thymus	thymus
13	chr4:110413200-110433800	Strong transcription	Dnd41	blood
14	chr4:110413400-110454800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:110415600-110428600	Strong transcription	HUVEC	blood vessel
16	chr4:110415600-110429000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr4:110416200-110454800	Weak transcription	Fetal Heart	heart
18	chr4:110416400-110452200	Weak transcription	Fetal Brain Male	brain
19	chr4:110416800-110449200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:110417000-110425200	Weak transcription	A549	lung
21	chr4:110417000-110429200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr4:110417000-110436600	Weak transcription	Aorta	Aorta
23	chr4:110417000-110440000	Weak transcription	Pancreas	Pancrea
24	chr4:110417000-110441800	Weak transcription	Right Ventricle	heart
25	chr4:110417000-110447400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr4:110417000-110448400	Weak transcription	Spleen	Spleen
27	chr4:110417000-110449200	Weak transcription	Hela-S3	cervix
28	chr4:110417000-110453400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr4:110417000-110453600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:110417000-110455800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr4:110417200-110441800	Weak transcription	Esophagus	oesophagus
32	chr4:110417200-110448400	Weak transcription	H9 Cell Line	embryonic stem cell
33	chr4:110417800-110433000	Weak transcription	Brain Hippocampus Middle	brain
34	chr4:110417800-110447400	Weak transcription	NHLF	lung
35	chr4:110418000-110428400	Weak transcription	Brain Anterior Caudate	brain
36	chr4:110418000-110428600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:110418000-110431000	Weak transcription	Brain Substantia Nigra	brain
38	chr4:110418200-110435000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr4:110418400-110448600	Weak transcription	Psoas Muscle	Psoas
40	chr4:110418600-110438000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr4:110418600-110438400	Weak transcription	Small Intestine	intestine
42	chr4:110418800-110429200	Weak transcription	Colon Smooth Muscle	Colon
43	chr4:110419000-110447400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr4:110419200-110432600	Weak transcription	K562	blood
45	chr4:110419200-110437400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
46	chr4:110419200-110438200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr4:110419400-110428200	Weak transcription	HepG2	liver
48	chr4:110419400-110431200	Weak transcription	NHEK	skin
49	chr4:110419400-110438400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
50	chr4:110420200-110466400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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