Variant report

Variant	rs73951514
Chromosome Location	chr18:39962583-39962584
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs60392901	1.00[AFR][1000 genomes]
rs60923905	1.00[AFR][1000 genomes]
rs7243805	0.84[AFR][1000 genomes]
rs73951505	1.00[AFR][1000 genomes]
rs73951506	1.00[AFR][1000 genomes]
rs73951508	0.92[AFR][1000 genomes]
rs73951510	0.92[AFR][1000 genomes]
rs73951513	0.83[AFR][1000 genomes]
rs73951553	1.00[AFR][1000 genomes]
rs73951554	1.00[AFR][1000 genomes]
rs73951579	0.92[AFR][1000 genomes]
rs73951588	0.92[AFR][1000 genomes]
rs73951598	0.84[AFR][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	nsv949609	chr18:39126941-40070286	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1059409	chr18:39711099-40139446	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv909572	chr18:39938510-40064000	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:39959600-39963600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr18:39961800-39964800	Weak transcription	H1 BMP4 Derived Mesendoderm 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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