Variant report

Variant	rs73875662
Chromosome Location	chr3:161279059-161279060
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1399914	1.00[AMR][1000 genomes]
rs16832749	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16832954	1.00[AMR][1000 genomes]
rs16832967	1.00[AMR][1000 genomes]
rs16833039	1.00[AMR][1000 genomes]
rs2135444	1.00[AMR][1000 genomes]
rs2135445	1.00[AMR][1000 genomes]
rs2135446	1.00[AMR][1000 genomes]
rs2135447	1.00[AMR][1000 genomes]
rs61535864	1.00[AMR][1000 genomes]
rs61710096	1.00[AMR][1000 genomes]
rs6774014	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6776579	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6787329	1.00[AMR][1000 genomes]
rs6798679	1.00[AMR][1000 genomes]
rs6802524	1.00[AMR][1000 genomes]
rs73875666	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73875668	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73875669	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73875671	1.00[AMR][1000 genomes]
rs73875672	1.00[AMR][1000 genomes]
rs73875679	1.00[AMR][1000 genomes]
rs73875680	1.00[AMR][1000 genomes]
rs73875682	1.00[AMR][1000 genomes]
rs73875699	1.00[AMR][1000 genomes]
rs73877415	1.00[AMR][1000 genomes]
rs73877416	1.00[AMR][1000 genomes]
rs73877419	1.00[AMR][1000 genomes]
rs73877424	1.00[AMR][1000 genomes]
rs73877439	1.00[AMR][1000 genomes]
rs73877445	1.00[AMR][1000 genomes]
rs7640549	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
2	nsv829773	chr3:161150422-161315189	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv829774	chr3:161229405-161386919	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2422309	chr3:161242389-161425932	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv877711	chr3:161275848-161486665	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161272800-161279600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr3:161276800-161280400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr3:161278000-161280600	Weak transcription	Dnd41	blood
4	chr3:161278400-161289400	Weak transcription	Colon Smooth Muscle	Colon

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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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