Variant report

Variant	rs251580
Chromosome Location	chr5:52487595-52487596
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:16)

rs_ID	r²[population]
rs152977	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs153119	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs153120	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs153121	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs153126	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs166129	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs251331	0.83[CHB][hapmap]
rs251505	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs251509	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs251512	1.00[CEU][hapmap];0.87[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs251517	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs254504	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs27316	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs27323	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs27324	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs774234	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949005	chr5:52188028-52808229	Flanking Bivalent TSS/Enh Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	esv2752745	chr5:52422063-53343529	Transcr. at gene 5' and 3' ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:52486000-52488200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:52486400-52491000	Enhancers	Hela-S3	cervix
3	chr5:52486600-52489600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr5:52487000-52487600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr5:52487000-52487600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr5:52487000-52487600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr5:52487000-52488200	Enhancers	NHLF	lung
8	chr5:52487200-52487600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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