Variant report

Variant	rs34741729
Chromosome Location	chr3:150604961-150604962
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs13069091	0.93[EUR][1000 genomes]
rs13074953	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13075078	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13075343	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13079392	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16862962	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16862966	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16862991	1.00[ASN][1000 genomes]
rs34110028	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34204678	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4234293	0.92[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs4680029	0.92[AFR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569140	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs569220	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59741456	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61360663	1.00[ASN][1000 genomes]
rs7619908	1.00[ASN][1000 genomes]
rs7649448	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7649543	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	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv877646	chr3:150582992-150641304	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150600200-150605400	Weak transcription	Primary monocytes fromperipheralblood	blood
2	chr3:150603200-150606200	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr3:150604600-150605000	Enhancers	Monocytes-CD14+_RO01746	blood
4	chr3:150604800-150605400	Enhancers	Foreskin Melanocyte Primary Cells skin03	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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