Variant report

Variant	rs1239702
Chromosome Location	chr13:51158084-51158085
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1239681	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1239682	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1239683	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239684	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239686	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239687	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239688	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239689	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239690	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239691	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1239692	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239693	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239695	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1239696	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1239703	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1239705	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1239706	0.83[ASN][1000 genomes]
rs1239707	0.84[ASN][1000 genomes]
rs1270717	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1271766	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2794469	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs706601	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs706602	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770383	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770384	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770385	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs770386	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs770388	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770391	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770392	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770393	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs770394	0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs770395	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs770396	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs947380	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs947382	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs947383	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9596313	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs978332	0.86[ASN][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	nsv1035151	chr13:50513535-51167850	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1254 gene(s)	inside rSNPs	diseases
2	esv2753964	chr13:50545399-51421199	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
3	esv2753492	chr13:50550081-51461720	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	1256 gene(s)	inside rSNPs	diseases
4	esv2753864	chr13:51136699-51375199	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:51147800-51160800	Weak transcription	Dnd41	blood
2	chr13:51149600-51162200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr13:51150400-51167400	Weak transcription	HepG2	liver
4	chr13:51150800-51160200	Weak transcription	Fetal Muscle Trunk	muscle
5	chr13:51151000-51161800	Weak transcription	Right Atrium	heart
6	chr13:51151200-51159000	Weak transcription	Left Ventricle	heart
7	chr13:51151200-51169600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr13:51155400-51158800	Weak transcription	NHDF-Ad	bronchial
9	chr13:51155400-51159000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:51155800-51159200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr13:51156000-51160000	Weak transcription	Right Ventricle	heart
12	chr13:51156200-51159000	Weak transcription	Osteobl	bone
13	chr13:51156200-51159200	Weak transcription	Fetal Stomach	stomach
14	chr13:51156200-51160000	Weak transcription	Fetal Thymus	thymus
15	chr13:51156200-51167600	Weak transcription	Fetal Kidney	kidney
16	chr13:51156400-51158800	Weak transcription	HSMMtube	muscle
17	chr13:51156400-51159000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr13:51156400-51159000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr13:51156800-51158400	Weak transcription	Fetal Muscle Leg	muscle
20	chr13:51157200-51159600	Weak transcription	Fetal Heart	heart

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