Variant report

Variant	rs58496096
Chromosome Location	chr1:152843491-152843492
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:152843289..152844260-chr1:153005064..153006050,2	MCF-7	breast:
2	chr1:152842063..152844434-chr1:153164775..153166274,11	MCF-7	breast:
3	chr1:152626130..152627645-chr1:152842015..152844012,15	MCF-7	breast:
4	chr1:152843080..152844798-chr1:153164828..153166213,18	MCF-7	breast:
5	chr1:152843310..152844245-chr1:152890638..152891212,2	MCF-7	breast:
6	chr1:152843263..152844168-chr1:153005237..153006058,6	MCF-7	breast:
7	chr1:152843206..152844266-chr1:152889921..152890796,3	MCF-7	breast:
8	chr1:152843390..152844417-chr1:152898307..152899295,4	MCF-7	breast:
9	chr1:152715224..152717554-chr1:152841619..152843723,2	MCF-7	breast:
10	chr1:152843465..152843985-chr20:45925441..45926105,2	MCF-7	breast:
11	chr1:152841334..152844015-chr1:152851385..152853978,2	K562	blood:
12	chr1:152843341..152844548-chr1:152897786..152899223,16	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 32 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10399610	1.00[AMR][1000 genomes]
rs10399676	1.00[AMR][1000 genomes]
rs10399731	1.00[AMR][1000 genomes]
rs12062507	1.00[AMR][1000 genomes]
rs12081158	1.00[AMR][1000 genomes]
rs12084353	1.00[AMR][1000 genomes]
rs12084482	1.00[AMR][1000 genomes]
rs12084802	1.00[AMR][1000 genomes]
rs12091343	1.00[AMR][1000 genomes]
rs12096212	1.00[AMR][1000 genomes]
rs4641263	1.00[AMR][1000 genomes]
rs56809825	1.00[AMR][1000 genomes]
rs56839988	1.00[AMR][1000 genomes]
rs57247972	1.00[AMR][1000 genomes]
rs58528923	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58759082	1.00[AMR][1000 genomes]
rs60809123	1.00[AMR][1000 genomes]
rs61113935	1.00[AMR][1000 genomes]
rs61500027	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757755	chr1:152472839-152898153	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv2758970	chr1:152472839-152898153	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv427786	chr1:152572990-152898153	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv1013433	chr1:152619305-153262215	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
5	nsv535170	chr1:152619305-153262215	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
6	nsv1001834	chr1:152648853-153279143	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
7	nsv547899	chr1:152672005-153245082	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
8	nsv999918	chr1:152749733-152861866	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1009885	chr1:152762750-152851273	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv1000159	chr1:152809514-152853766	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1008447	chr1:152811171-152853748	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv2761937	chr1:152811183-152853760	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv831592	chr1:152815054-152997162	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152838800-152846000	Weak transcription	HMEC	breast
2	chr1:152839200-152843800	Weak transcription	NHEK	skin
3	chr1:152840600-152843600	Weak transcription	Fetal Stomach	stomach
4	chr1:152843200-152844000	Enhancers	GM12878-XiMat	blood
5	chr1:152843400-152844000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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