Variant report

Variant	rs342603
Chromosome Location	chr5:106883678-106883679
allele	A/T
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:18)

rs_ID	r²[population]
rs163727	0.91[CHB][hapmap]
rs164699	0.86[CHB][hapmap]
rs2161514	0.87[CHB][hapmap]
rs2445074	0.92[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2484103	0.87[CHB][hapmap]
rs341272	0.88[CEU][hapmap];0.91[CHB][hapmap];0.94[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs342604	0.91[CHB][hapmap]
rs352609	0.95[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs41375	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs445747	0.87[CHB][hapmap]
rs459400	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs459637	0.91[CHB][hapmap]
rs464950	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs467089	1.00[CHB][hapmap];0.88[JPT][hapmap];0.99[ASN][1000 genomes]
rs553363	0.91[CHB][hapmap]
rs555989	0.91[CHB][hapmap]
rs662627	0.95[CHB][hapmap]
rs677797	0.91[CHB][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1034276	chr5:106461538-106944163	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv537851	chr5:106461538-106944163	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
3	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:49 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:106875000-106885200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr5:106878800-106891600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr5:106879000-106884400	Weak transcription	HSMMtube	muscle
4	chr5:106879000-106884400	Weak transcription	NHDF-Ad	bronchial
5	chr5:106879000-106893000	Weak transcription	Psoas Muscle	Psoas
6	chr5:106879000-106899200	Weak transcription	Fetal Stomach	stomach
7	chr5:106879200-106884200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr5:106879400-106884400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr5:106879400-106888200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:106879400-106888800	Weak transcription	HMEC	breast
11	chr5:106879600-106888000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr5:106879800-106884600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr5:106879800-106887800	Weak transcription	NHLF	lung
14	chr5:106879800-106888800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr5:106880000-106885200	Weak transcription	Esophagus	oesophagus
16	chr5:106880200-106884600	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr5:106880200-106884600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr5:106880200-106885200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr5:106880200-106889000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr5:106880400-106884400	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr5:106880400-106884600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr5:106880400-106885200	Weak transcription	Aorta	Aorta
23	chr5:106880400-106885400	Weak transcription	Pancreas	Pancrea
24	chr5:106880600-106886800	Weak transcription	Right Ventricle	heart
25	chr5:106880800-106884200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
26	chr5:106881200-106884400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr5:106881400-106884400	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr5:106881400-106885200	Weak transcription	Right Atrium	heart
29	chr5:106881400-106888600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:106881400-106889000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr5:106881600-106899600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr5:106882200-106885200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr5:106882200-106885200	Weak transcription	Left Ventricle	heart
34	chr5:106882600-106884600	Enhancers	Dnd41	blood
35	chr5:106882600-106885800	Enhancers	A549	lung
36	chr5:106882800-106884600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr5:106882800-106885200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:106883000-106884200	Weak transcription	HSMM	muscle
39	chr5:106883000-106885400	Weak transcription	Brain Angular Gyrus	brain
40	chr5:106883000-106888600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr5:106883200-106884200	Weak transcription	Thymus	Thymus
42	chr5:106883200-106884800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr5:106883200-106886800	Weak transcription	Fetal Lung	lung
44	chr5:106883400-106883800	Weak transcription	Fetal Heart	heart
45	chr5:106883400-106884600	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr5:106883400-106884800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr5:106883400-106885000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr5:106883400-106890000	Weak transcription	Pancreatic Islets	Pancreatic Islet
49	chr5:106883600-106884400	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links