Variant report

Variant	rs73868734
Chromosome Location	chr3:139850285-139850286
allele	G/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:15)

rs_ID	r²[population]
rs16849961	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16849965	1.00[AMR][1000 genomes]
rs16849989	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56865323	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56910077	1.00[AMR][1000 genomes]
rs58668644	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59327241	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60452039	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60537808	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61547225	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73868736	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73868739	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73868740	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73868761	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73868777	0.97[AFR][1000 genomes];1.00[AMR][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	nsv998423	chr3:139526446-139947336	Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv829738	chr3:139670836-139851945	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv829739	chr3:139797496-140002685	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:139835800-139862800	Weak transcription	HSMMtube	muscle
2	chr3:139842600-139854200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:139848200-139850400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:139849200-139850400	Weak transcription	Right Atrium	heart

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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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