Variant report

Variant	rs3099513
Chromosome Location	chr13:85207783-85207784
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1374411	0.86[AMR][1000 genomes]
rs1374412	0.86[AMR][1000 genomes]
rs1446793	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1867900	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1867901	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2100084	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4075134	0.84[AMR][1000 genomes]
rs4605042	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs55875665	0.86[AMR][1000 genomes]
rs67116577	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67564213	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs67648125	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs72629431	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7322072	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7322166	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs9602507	1.00[ASN][1000 genomes]
rs977180	0.82[AMR][1000 genomes];0.83[EUR][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	nsv949402	chr13:84675752-85606846	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv456046	chr13:84971270-85262508	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv562561	chr13:84971270-85262508	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv900691	chr13:85206473-85294881	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	esv1851778	chr13:85206473-85299207	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85200200-85211400	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