Variant report

Variant	rs1647391
Chromosome Location	chr15:57102522-57102523
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:57098196..57100093-chr15:57101198..57103621,2	K562	blood:
2	chr15:57102473..57104641-chr15:57108016..57110704,2	K562	blood:

Extended variants
information (count: 60 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10518872	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11071285	0.89[EUR][1000 genomes]
rs12437635	0.85[AMR][1000 genomes]
rs12437714	0.88[AMR][1000 genomes]
rs12437735	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12438377	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12438572	0.82[AMR][1000 genomes]
rs12438728	0.89[EUR][1000 genomes]
rs12439116	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12439563	0.89[EUR][1000 genomes]
rs12439697	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12440006	0.89[EUR][1000 genomes]
rs12440725	0.84[AMR][1000 genomes]
rs12440891	0.80[AMR][1000 genomes]
rs12441746	0.84[EUR][1000 genomes]
rs12441769	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12441792	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12442069	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12442630	0.88[AMR][1000 genomes]
rs12442642	0.80[AMR][1000 genomes]
rs12442662	0.84[AMR][1000 genomes]
rs12442839	0.80[AMR][1000 genomes]
rs12443178	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12903143	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12907983	0.89[EUR][1000 genomes]
rs1364541	0.88[AMR][1000 genomes]
rs1529597	0.84[AMR][1000 genomes]
rs1600829	0.89[EUR][1000 genomes]
rs1600831	0.84[EUR][1000 genomes]
rs1631905	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1647386	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16977123	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17238880	0.83[EUR][1000 genomes]
rs17238894	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17238901	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17238950	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17819592	0.89[EUR][1000 genomes]
rs17819616	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17819646	0.84[AMR][1000 genomes]
rs17819658	0.80[AMR][1000 genomes]
rs17819664	0.80[AMR][1000 genomes]
rs1834199	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2052641	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2161935	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2899599	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4287503	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4362334	0.84[AMR][1000 genomes]
rs4424865	0.88[AMR][1000 genomes]
rs4774885	0.89[EUR][1000 genomes]
rs480701	0.89[EUR][1000 genomes]
rs6493888	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7176472	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs74015901	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs966807	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3422474	chr15:56867190-57244330	Strong transcription ZNF genes & repeats Active TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv569576	chr15:57012816-57126917	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv833020	chr15:57055947-57216068	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv457162	chr15:57083006-57225766	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
5	nsv569577	chr15:57083006-57225766	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
6	nsv1042486	chr15:57094598-57505992	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57091200-57104200	Weak transcription	Aorta	Aorta
2	chr15:57099000-57104200	Weak transcription	Ovary	ovary
3	chr15:57100000-57102600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:57100200-57114000	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:57100400-57111600	Weak transcription	Thymus	Thymus
6	chr15:57100800-57104000	Weak transcription	Fetal Lung	lung
7	chr15:57102200-57109200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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