Variant report

Variant	rs73158545
Chromosome Location	chr3:157224461-157224462
allele	C/T
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]
rs10513515	0.90[EUR][1000 genomes]
rs35973239	0.86[EUR][1000 genomes]
rs58178116	0.90[EUR][1000 genomes]
rs73158534	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs73158539	0.86[EUR][1000 genomes]
rs73158547	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73158549	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73158550	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73158551	1.00[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs73158557	1.00[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs73158591	1.00[AFR][1000 genomes]
rs73160604	1.00[AFR][1000 genomes]
rs73160606	1.00[AFR][1000 genomes]
rs73160607	1.00[AFR][1000 genomes]
rs73160608	1.00[AFR][1000 genomes]
rs73160612	1.00[AFR][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	esv2757900	chr3:157090166-157254684	Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	esv2759193	chr3:157090166-157254684	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:157217800-157235400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr3:157221800-157226000	Weak transcription	Osteobl	bone
3	chr3:157221800-157244800	Weak transcription	NH-A	brain
4	chr3:157222600-157241800	Weak transcription	HSMM	muscle
5	chr3:157223200-157239000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:157224400-157227400	Weak transcription	HUVEC	blood vessel

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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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