Variant report

Variant	rs2531151
Chromosome Location	chr4:15909533-15909534
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs2098055	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2532068	0.95[EUR][1000 genomes]
rs73116477	1.00[EUR][1000 genomes]
rs73116482	1.00[EUR][1000 genomes]
rs73116488	0.93[EUR][1000 genomes]
rs73116493	1.00[EUR][1000 genomes]
rs73118457	1.00[EUR][1000 genomes]
rs73118459	1.00[EUR][1000 genomes]
rs73118460	1.00[EUR][1000 genomes]
rs73118463	0.95[EUR][1000 genomes]
rs73118466	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv916742	chr4:15797994-16064232	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv878715	chr4:15840839-15947493	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15908000-15909600	Enhancers	Fetal Stomach	stomach
2	chr4:15908200-15911800	Weak transcription	Esophagus	oesophagus
3	chr4:15908200-15913800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr4:15908400-15912600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr4:15908400-15913800	Weak transcription	Placenta	Placenta
6	chr4:15908600-15909600	Enhancers	Rectal Smooth Muscle	rectum
7	chr4:15908600-15914200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:15908800-15909600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:15909000-15909600	Weak transcription	NHEK	skin
10	chr4:15909000-15909800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr4:15909000-15912000	Weak transcription	Hela-S3	cervix
12	chr4:15909000-15913600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr4:15909200-15909600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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Input of quick search could be:

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

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