Variant report

Variant	rs7171510
Chromosome Location	chr15:33433907-33433908
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12902884	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12903814	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12915870	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16965470	0.98[EUR][1000 genomes]
rs17816892	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17816898	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17816904	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34633722	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35060601	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35187364	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35493298	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35695671	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35836585	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35991626	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36010988	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs36014025	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs71462852	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs71462853	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7173052	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv903983	chr15:33388030-33550256	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33420600-33434800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:33424400-33440600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:33427800-33445400	Weak transcription	Right Atrium	heart
4	chr15:33430600-33434400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr15:33433600-33434200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr15:33433600-33436200	Enhancers	Fetal Intestine Small	intestine
7	chr15:33433600-33436600	Enhancers	Fetal Intestine Large	intestine
8	chr15:33433800-33434200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr15:33433800-33434200	Enhancers	Lung	lung

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dbSNP/dbVar ID: rs12345 /nsv7879
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