Variant report

Variant	rs62135195
Chromosome Location	chr2:48760179-48760180
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17325558	0.95[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62135175	0.88[EUR][1000 genomes]
rs62135196	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62135197	0.86[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6721913	0.83[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6750122	0.81[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005954	chr2:48692696-48905723	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats 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
2	nsv535682	chr2:48692696-48905723	Weak transcription Strong transcription Enhancers Flanking Active TSS 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	9 gene(s)	inside rSNPs	diseases
3	nsv833981	chr2:48705444-48878179	ZNF genes & repeats Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1007491	chr2:48752185-48796441	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv535683	chr2:48752185-48796441	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:48758000-48766000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:48758600-48762000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr2:48758600-48762200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr2:48758800-48760200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr2:48758800-48760200	Enhancers	Placenta	Placenta
6	chr2:48758800-48761800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:48758800-48762000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr2:48758800-48769000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr2:48758800-48772400	Weak transcription	Fetal Muscle Trunk	muscle
10	chr2:48759000-48760200	Enhancers	Adipose Nuclei	Adipose
11	chr2:48759000-48760200	Enhancers	HUVEC	blood vessel
12	chr2:48759000-48760400	Enhancers	Left Ventricle	heart
13	chr2:48759000-48761600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr2:48759000-48761800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr2:48759000-48762000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr2:48759000-48765200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:48759000-48765400	Weak transcription	HUES64 Cell Line	embryonic stem cell
18	chr2:48759000-48772600	Weak transcription	Fetal Muscle Leg	muscle
19	chr2:48759000-48775200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr2:48759000-48787000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr2:48759000-48787400	Weak transcription	Psoas Muscle	Psoas
22	chr2:48759000-48827600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:48759200-48760200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr2:48759200-48760200	Enhancers	Colon Smooth Muscle	Colon
25	chr2:48759200-48760400	Weak transcription	Fetal Intestine Small	intestine
26	chr2:48759200-48760400	Enhancers	Ovary	ovary
27	chr2:48759200-48766000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr2:48759200-48767000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr2:48759200-48793200	Weak transcription	Fetal Lung	lung
30	chr2:48759400-48760200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr2:48759400-48762600	Weak transcription	Fetal Intestine Large	intestine
32	chr2:48759400-48767000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr2:48759400-48775200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr2:48759800-48760200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr2:48759800-48760200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr2:48759800-48760200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr2:48759800-48760200	Flanking Active TSS	Rectal Smooth Muscle	rectum
38	chr2:48759800-48760200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr2:48759800-48760200	Enhancers	Spleen	Spleen
40	chr2:48760000-48760200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr2:48760000-48760200	Enhancers	Stomach Smooth Muscle	stomach
42	chr2:48760000-48760200	Enhancers	NHDF-Ad	bronchial
43	chr2:48760000-48761800	Weak transcription	Fetal Stomach	stomach
44	chr2:48760000-48766200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr2:48760000-48770800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr2:48760000-48771000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr2:48760000-48772000	Weak transcription	Lung	lung
48	chr2:48760000-48772400	Weak transcription	Right Atrium	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links