Variant report

Variant	rs6865036
Chromosome Location	chr5:147750725-147750726
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:147749453..147751335-chr5:147809233..147810994,2	K562	blood:

Variant related genes	Relation type
ENSG00000251330	Chromatin interaction

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10036053	0.89[EUR][1000 genomes]
rs10037318	0.95[EUR][1000 genomes]
rs10044054	0.88[EUR][1000 genomes]
rs10050560	0.89[EUR][1000 genomes]
rs10057472	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10060180	0.82[EUR][1000 genomes]
rs10068891	0.85[EUR][1000 genomes]
rs10072817	0.91[EUR][1000 genomes]
rs10072958	0.91[EUR][1000 genomes]
rs10476892	0.87[EUR][1000 genomes]
rs10477374	0.88[EUR][1000 genomes]
rs10515610	0.95[EUR][1000 genomes]
rs12516267	0.92[EUR][1000 genomes]
rs12519039	0.94[EUR][1000 genomes]
rs12521065	0.95[EUR][1000 genomes]
rs12717971	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13153619	0.87[EUR][1000 genomes]
rs13157347	0.91[EUR][1000 genomes]
rs13158948	0.87[EUR][1000 genomes]
rs13176114	0.85[EUR][1000 genomes]
rs13358385	0.94[EUR][1000 genomes]
rs1345741	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1363704	0.89[EUR][1000 genomes]
rs1363705	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1363707	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1422968	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1422970	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1422977	0.84[EUR][1000 genomes]
rs1582519	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs17719578	0.85[EUR][1000 genomes]
rs17719662	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17719763	0.90[EUR][1000 genomes]
rs17719873	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17776554	0.94[EUR][1000 genomes]
rs17776674	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1862430	0.85[EUR][1000 genomes]
rs1862431	0.89[EUR][1000 genomes]
rs2161432	0.87[EUR][1000 genomes]
rs2216653	0.87[EUR][1000 genomes]
rs2400509	0.85[EUR][1000 genomes]
rs2400510	0.85[EUR][1000 genomes]
rs28442279	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2895761	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34001290	0.86[EUR][1000 genomes]
rs34163281	0.85[EUR][1000 genomes]
rs35006442	0.85[EUR][1000 genomes]
rs35700061	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs35792476	0.85[EUR][1000 genomes]
rs3749689	0.89[EUR][1000 genomes]
rs3749690	0.85[EUR][1000 genomes]
rs4406123	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4705247	0.82[EUR][1000 genomes]
rs4705248	0.91[EUR][1000 genomes]
rs4705249	0.89[EUR][1000 genomes]
rs4705251	0.93[EUR][1000 genomes]
rs4705252	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6580542	0.85[EUR][1000 genomes]
rs6580544	0.90[EUR][1000 genomes]
rs6580545	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6580546	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6580548	0.88[EUR][1000 genomes]
rs6860261	0.86[EUR][1000 genomes]
rs6865972	0.86[EUR][1000 genomes]
rs6866106	0.88[EUR][1000 genomes]
rs6875252	0.85[EUR][1000 genomes]
rs6875795	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6876308	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6876982	0.89[EUR][1000 genomes]
rs6882932	0.84[EUR][1000 genomes]
rs6886203	0.89[EUR][1000 genomes]
rs6891724	0.88[EUR][1000 genomes]
rs6892647	0.90[EUR][1000 genomes]
rs6893378	0.86[EUR][1000 genomes]
rs6894032	0.87[EUR][1000 genomes]
rs7712350	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7713986	0.85[EUR][1000 genomes]
rs7716578	0.88[EUR][1000 genomes]
rs7722458	0.95[EUR][1000 genomes]
rs7729309	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7730707	0.90[EUR][1000 genomes]
rs7731526	0.94[EUR][1000 genomes]
rs7734458	0.85[EUR][1000 genomes]
rs7736728	0.87[EUR][1000 genomes]
rs9325094	0.95[EUR][1000 genomes]
rs9784645	0.86[EUR][1000 genomes]
rs999741	0.87[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	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147723600-147751600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:147729200-147762200	Weak transcription	Aorta	Aorta
3	chr5:147730200-147754200	Weak transcription	Left Ventricle	heart
4	chr5:147747800-147762400	Weak transcription	Ovary	ovary
5	chr5:147748200-147756800	Weak transcription	Fetal Brain Female	brain
6	chr5:147749600-147757400	Weak transcription	Psoas Muscle	Psoas
7	chr5:147749800-147757400	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr5:147749800-147762200	Weak transcription	Adipose Nuclei	Adipose
9	chr5:147750000-147756600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr5:147750000-147762400	Weak transcription	Brain Substantia Nigra	brain
11	chr5:147750400-147756600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr5:147750600-147752600	Strong transcription	Brain Germinal Matrix	brain

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