Variant report

Variant	rs73680595
Chromosome Location	chr8:58785067-58785068
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10504248	1.00[ASN][1000 genomes]
rs1369771	1.00[ASN][1000 genomes]
rs1369772	1.00[ASN][1000 genomes]
rs1436018	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16918685	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16922716	1.00[ASN][1000 genomes]
rs2082912	1.00[ASN][1000 genomes]
rs2099520	1.00[ASN][1000 genomes]
rs55774155	1.00[ASN][1000 genomes]
rs58879638	1.00[ASN][1000 genomes]
rs6471659	1.00[ASN][1000 genomes]
rs6992698	1.00[ASN][1000 genomes]
rs73683803	1.00[ASN][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	nsv533217	chr8:57991065-58789001	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv831323	chr8:58692548-58849862	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:58777600-58785800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:58780000-58789000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr8:58781600-58785600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links