Variant report

Variant	rs58925493
Chromosome Location	chr4:90608142-90608143
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs35522252	1.00[AMR][1000 genomes]
rs55678476	1.00[AFR][1000 genomes]
rs73830646	0.83[AFR][1000 genomes]
rs73830650	0.83[AFR][1000 genomes]
rs73830657	0.83[AFR][1000 genomes]
rs73834318	1.00[AMR][1000 genomes]
rs73834320	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470051	chr4:89644931-90643144	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
2	esv2830400	chr4:90085456-90922432	Flanking Active TSS Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv879535	chr4:90565218-90624853	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
6	nsv461578	chr4:90572322-90624853	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
7	nsv461579	chr4:90572322-90624853	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
8	nsv594818	chr4:90572322-90624853	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
9	nsv461580	chr4:90572322-90630901	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
10	nsv594819	chr4:90572322-90630901	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
11	nsv522681	chr4:90603044-90630901	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:90604200-90608400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr4:90604200-90608600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:90604400-90616200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr4:90604800-90608400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
5	chr4:90604800-90609000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr4:90605800-90611200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:90606200-90608800	Strong transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:90606400-90608200	Strong transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:90606400-90608200	Enhancers	Primary T cells from cord blood	blood
10	chr4:90606400-90608400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:90607000-90609000	Weak transcription	HepG2	liver
12	chr4:90607200-90608400	Enhancers	Dnd41	blood
13	chr4:90607200-90610400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:90607200-90624800	Weak transcription	NHEK	skin
15	chr4:90607400-90609800	Strong transcription	HMEC	breast
16	chr4:90607400-90610200	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr4:90607400-90610400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr4:90607400-90610600	Weak transcription	HUES48 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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