Variant report

Variant	rs73845111
Chromosome Location	chr3:84852538-84852539
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs17022263	1.00[AMR][1000 genomes]
rs4470448	1.00[AMR][1000 genomes]
rs56152547	1.00[AMR][1000 genomes]
rs56328407	1.00[AMR][1000 genomes]
rs60626147	0.90[AFR][1000 genomes]
rs60728740	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73842813	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73842820	1.00[AMR][1000 genomes]
rs73842821	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73842822	1.00[AMR][1000 genomes]
rs73842856	1.00[AMR][1000 genomes]
rs73843248	1.00[AMR][1000 genomes]
rs73843249	1.00[AMR][1000 genomes]
rs73843250	1.00[AMR][1000 genomes]
rs73843251	1.00[AMR][1000 genomes]
rs73843255	1.00[AMR][1000 genomes]
rs73843257	1.00[AMR][1000 genomes]
rs73843259	1.00[AMR][1000 genomes]
rs73843260	1.00[AMR][1000 genomes]
rs73845110	0.90[AFR][1000 genomes]
rs73845112	0.88[AFR][1000 genomes]
rs73845113	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73845547	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	esv3381298	chr3:84689266-85030314	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1002058	chr3:84757044-85389876	Bivalent Enhancer Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1001316	chr3:84773522-85071342	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv877085	chr3:84779079-84911212	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv590895	chr3:84838638-84940927	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:84845200-84856400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

Quick Search:

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

what's new

Quick links