Variant report

Variant	rs7650615
Chromosome Location	chr3:140636790-140636791
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:140630903..140633171-chr3:140636198..140638859,2	K562	blood:
2	chr3:140625666..140627502-chr3:140635151..140637748,2	K562	blood:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs1056127	0.83[CHB][hapmap]
rs12486226	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12491336	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1519191	0.98[EUR][1000 genomes]
rs1519192	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1519194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1568338	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56683057	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59222505	0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60354869	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6769114	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6793318	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72989087	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72989089	0.98[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs72989090	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72989093	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72989095	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs72989097	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72989101	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72991013	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72991014	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72991016	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72991017	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72991019	0.85[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs7624649	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7625667	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7628638	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7628654	1.00[EUR][1000 genomes];0.92[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	nsv591865	chr3:140396022-140728850	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1005522	chr3:140454632-140685915	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv536732	chr3:140454632-140685915	Strong transcription Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140635600-140637000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:140635800-140637400	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr3:140635800-140637400	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr3:140635800-140638000	Enhancers	Pancreas	Pancrea
5	chr3:140636200-140636800	Enhancers	Left Ventricle	heart
6	chr3:140636200-140637000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr3:140636200-140637000	Enhancers	Psoas Muscle	Psoas
8	chr3:140636400-140636800	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr3:140636400-140636800	Enhancers	Right Atrium	heart
10	chr3:140636400-140637000	Enhancers	Fetal Intestine Large	intestine
11	chr3:140636400-140637000	Enhancers	HepG2	liver
12	chr3:140636400-140637200	Enhancers	Fetal Intestine Small	intestine
13	chr3:140636600-140636800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr3:140636600-140637000	Bivalent Enhancer	Liver	Liver
15	chr3:140636600-140637200	Active TSS	Duodenum Mucosa	Duodenum

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