Variant report

Variant	rs74018958
Chromosome Location	chr15:58440168-58440169
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	chr15:58433881..58435963-chr15:58440042..58441729,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs56114312	1.00[AMR][1000 genomes]
rs56787487	1.00[AMR][1000 genomes]
rs57297157	1.00[AMR][1000 genomes]
rs57557175	1.00[AMR][1000 genomes]
rs57882243	1.00[AMR][1000 genomes]
rs59302780	1.00[AMR][1000 genomes]
rs60201017	1.00[AMR][1000 genomes]
rs74015811	1.00[AMR][1000 genomes]
rs74016540	1.00[AMR][1000 genomes]
rs74016543	1.00[AMR][1000 genomes]
rs74016574	1.00[AMR][1000 genomes]
rs74016575	1.00[AMR][1000 genomes]
rs74016576	1.00[AMR][1000 genomes]
rs74016578	1.00[AMR][1000 genomes]
rs74016579	1.00[AMR][1000 genomes]
rs74016580	1.00[AMR][1000 genomes]
rs74016581	1.00[AMR][1000 genomes]
rs74016584	1.00[AMR][1000 genomes]
rs74016585	1.00[AMR][1000 genomes]
rs74016586	1.00[AMR][1000 genomes]
rs74016589	1.00[AMR][1000 genomes]
rs74016590	1.00[AMR][1000 genomes]
rs74016591	1.00[AMR][1000 genomes]
rs74018015	1.00[AMR][1000 genomes]
rs74018016	1.00[AMR][1000 genomes]
rs74018017	1.00[AMR][1000 genomes]
rs74018020	1.00[AMR][1000 genomes]
rs74018027	1.00[AMR][1000 genomes]
rs74018028	1.00[AMR][1000 genomes]
rs74018035	1.00[AMR][1000 genomes]
rs74018817	1.00[AMR][1000 genomes]
rs74018826	1.00[AMR][1000 genomes]
rs74018834	1.00[AMR][1000 genomes]
rs74018836	1.00[AMR][1000 genomes]
rs74018844	1.00[AMR][1000 genomes]
rs74018846	1.00[AMR][1000 genomes]
rs74018847	1.00[AMR][1000 genomes]
rs74018848	1.00[AMR][1000 genomes]
rs74018850	1.00[AMR][1000 genomes]
rs74018851	1.00[AMR][1000 genomes]
rs74018954	1.00[AMR][1000 genomes]
rs74018956	1.00[AMR][1000 genomes]
rs8037139	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038667	chr15:57933076-58481870	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv542400	chr15:57933076-58481870	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv1047246	chr15:58375607-58707158	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv457172	chr15:58417895-58457507	Enhancers Weak transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv569597	chr15:58417895-58457507	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr15:58433400-58441800	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr15:58433800-58442400	Weak transcription	Aorta	Aorta
3	chr15:58438200-58441800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr15:58438600-58441600	Enhancers	Fetal Kidney	kidney
5	chr15:58438800-58441600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr15:58438800-58441600	Enhancers	Liver	Liver
7	chr15:58439400-58440200	Weak transcription	Primary B cells from cord blood	blood
8	chr15:58439400-58442400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:58439600-58440600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr15:58439600-58441400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
11	chr15:58439800-58440600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr15:58439800-58441000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr15:58440000-58440400	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr15:58440000-58441000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr15:58440000-58441000	Weak transcription	Primary hematopoietic stem cells	blood

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