Variant report

Variant	rs11675814
Chromosome Location	chr2:134335992-134335993
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11688182	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1368096	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17816830	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1864816	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1864817	0.94[ASN][1000 genomes]
rs34522146	0.93[AFR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34570953	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34720835	0.94[ASN][1000 genomes]
rs4954068	0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6430432	0.90[EUR][1000 genomes]
rs6710186	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6715224	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6723321	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997821	chr2:133868822-134360220	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
2	nsv535927	chr2:133868822-134360220	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
3	nsv1003624	chr2:134126928-134583203	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv1006101	chr2:134263288-134973917	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
5	nsv516644	chr2:134301130-134391214	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv431713	chr2:134316522-134413604	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1013713	chr2:134322236-134644574	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv535931	chr2:134322236-134644574	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:134325000-134342400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:134326200-134337000	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr2:134326400-134336200	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr2:134326400-134337000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr2:134326600-134336000	Weak transcription	Brain Anterior Caudate	brain
6	chr2:134326600-134344200	Weak transcription	Brain Cingulate Gyrus	brain
7	chr2:134330200-134339800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
8	chr2:134332000-134339000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr2:134332200-134339800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:134332600-134338800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr2:134332600-134338800	Weak transcription	Right Atrium	heart
12	chr2:134332800-134336200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr2:134332800-134336600	Weak transcription	NH-A	brain
14	chr2:134332800-134336800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:134332800-134337000	Weak transcription	Brain Hippocampus Middle	brain
16	chr2:134332800-134337000	Weak transcription	Fetal Muscle Leg	muscle
17	chr2:134333800-134338800	Weak transcription	Pancreas	Pancrea
18	chr2:134334600-134336800	Weak transcription	NHDF-Ad	bronchial
19	chr2:134334600-134338800	Weak transcription	Right Ventricle	heart
20	chr2:134334800-134336000	Weak transcription	Fetal Heart	heart
21	chr2:134334800-134336200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr2:134334800-134336600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr2:134334800-134336600	Weak transcription	NHLF	lung
24	chr2:134335000-134336000	Weak transcription	Liver	Liver
25	chr2:134335000-134336000	Weak transcription	Stomach Mucosa	stomach
26	chr2:134335000-134336200	Weak transcription	NHEK	skin
27	chr2:134335000-134336200	Weak transcription	Osteobl	bone
28	chr2:134335000-134336400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr2:134335000-134336400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr2:134335000-134336400	Weak transcription	HMEC	breast
31	chr2:134335000-134336600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr2:134335000-134336600	Weak transcription	A549	lung
33	chr2:134335000-134343800	Weak transcription	Esophagus	oesophagus
34	chr2:134335400-134337800	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr2:134335600-134337600	Enhancers	Hela-S3	cervix
36	chr2:134335600-134340000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr2:134335600-134340000	Enhancers	HUVEC	blood vessel
38	chr2:134335800-134336000	Enhancers	Gastric	stomach
39	chr2:134335800-134336200	Enhancers	Lung	lung
40	chr2:134335800-134337600	Enhancers	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links