Variant report

Variant	rs255863
Chromosome Location	chr5:112747153-112747154
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs10067046	0.85[AMR][1000 genomes]
rs13190054	0.83[AMR][1000 genomes]
rs1517208	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1517210	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs154039	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs154040	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs164251	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs171181	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs173903	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs182987	0.82[AMR][1000 genomes]
rs1838207	0.82[AMR][1000 genomes]
rs1845290	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs190453	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2431548	0.82[AMR][1000 genomes]
rs2434664	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs255856	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs255858	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs255867	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs255874	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs26960	0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs26983	0.86[AMR][1000 genomes]
rs26985	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs26987	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs26988	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs27566	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs27700	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs348927	0.82[EUR][1000 genomes]
rs348933	0.82[AMR][1000 genomes]
rs348949	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs348950	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs348953	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs36612	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3857435	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs406288	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs423089	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4324667	0.90[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs459428	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs461034	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs463216	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs465898	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs466564	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4705813	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6594711	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs675353	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs6869097	0.93[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs6875238	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6879612	0.91[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7702120	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7715342	0.83[AMR][1000 genomes]
rs7722276	0.83[AMR][1000 genomes]
rs9686772	0.82[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv599396	chr5:112408944-112853189	Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 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	chr5:112724400-112751200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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