Variant report

Variant	rs35721910
Chromosome Location	chr8:130106192-130106193
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:130101158..130103152-chr8:130105792..130107982,2	K562	blood:

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10105449	0.90[EUR][1000 genomes]
rs10435553	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10435554	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10435555	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10448000	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10956463	0.81[AFR][1000 genomes]
rs1157275	0.85[EUR][1000 genomes]
rs12541644	0.99[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12541935	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12543251	0.91[ASN][1000 genomes]
rs13279328	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1372442	0.85[EUR][1000 genomes]
rs1372443	0.85[EUR][1000 genomes]
rs1372453	0.88[EUR][1000 genomes]
rs34294444	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34294531	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34495693	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34871599	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs34892339	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35658327	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4236737	0.85[EUR][1000 genomes]
rs4302810	0.85[EUR][1000 genomes]
rs4333552	0.84[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs4371972	0.85[EUR][1000 genomes]
rs4448233	0.83[AFR][1000 genomes]
rs4493878	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4526322	0.81[EUR][1000 genomes]
rs4566994	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4613963	0.92[EUR][1000 genomes]
rs4636163	0.92[EUR][1000 genomes]
rs4644199	0.84[EUR][1000 genomes]
rs57797099	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59669561	0.91[ASN][1000 genomes]
rs6470676	0.85[EUR][1000 genomes]
rs6470677	0.85[EUR][1000 genomes]
rs6470692	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6470694	0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs66879839	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67401439	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67459926	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6989490	0.85[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6996806	0.87[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7004935	0.85[ASN][1000 genomes]
rs73382040	0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73382043	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7815639	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7815753	0.81[AFR][1000 genomes]
rs7816364	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7820114	0.84[EUR][1000 genomes]
rs7832166	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7832400	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7832457	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7832834	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7833157	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7834731	0.90[EUR][1000 genomes]
rs7836429	0.84[EUR][1000 genomes]
rs7839556	0.82[AMR][1000 genomes]
rs7840107	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7843664	0.89[EUR][1000 genomes]
rs9650100	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9650101	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv891442	chr8:130016499-130130604	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv891443	chr8:130016499-130220746	Weak transcription Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv891444	chr8:130024642-130130604	Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130085600-130115200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:130094800-130112000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr8:130102400-130107200	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr8:130105800-130108400	Genic enhancers	Dnd41	blood
5	chr8:130106000-130107000	Strong transcription	Fetal Thymus	thymus

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