Variant report

Variant	rs10485211
Chromosome Location	chr6:73240002-73240003
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:73239217..73240861-chr6:73262225..73264019,2	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs10085254	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10214605	1.00[ASN][1000 genomes]
rs10485210	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1147534	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1147536	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1147537	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1147538	0.94[EUR][1000 genomes]
rs1147540	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1202107	1.00[CEU][hapmap]
rs1202110	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1202117	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1202118	0.94[EUR][1000 genomes]
rs1202120	0.94[EUR][1000 genomes]
rs1202121	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1202122	0.94[EUR][1000 genomes]
rs1334345	0.88[EUR][1000 genomes]
rs1590801	1.00[CEU][hapmap];0.80[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16882468	0.92[EUR][1000 genomes]
rs16882473	0.96[EUR][1000 genomes]
rs16882476	0.94[EUR][1000 genomes]
rs16882487	1.00[CEU][hapmap]
rs16882500	1.00[CEU][hapmap]
rs16882506	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16882539	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4307137	0.96[EUR][1000 genomes]
rs55739455	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59106883	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs59352656	0.96[EUR][1000 genomes]
rs61032405	0.96[EUR][1000 genomes]
rs66805874	0.86[EUR][1000 genomes]
rs68186765	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6909267	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72939319	0.92[EUR][1000 genomes]
rs72941783	0.88[EUR][1000 genomes]
rs72941788	0.88[EUR][1000 genomes]
rs72943183	0.96[EUR][1000 genomes]
rs72946182	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72946193	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72948113	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9442816	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9442819	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9446671	1.00[ASN][1000 genomes]
rs9446695	1.00[ASN][1000 genomes]
rs9446696	1.00[ASN][1000 genomes]
rs9446697	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446701	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9446703	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9446704	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9446705	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023809	chr6:73157813-73477997	Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv538303	chr6:73157813-73477997	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73232800-73243000	Weak transcription	K562	blood
2	chr6:73236000-73242800	Weak transcription	HSMMtube	muscle
3	chr6:73236200-73241400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr6:73236200-73242200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:73239600-73241600	Enhancers	NHEK	skin
6	chr6:73239600-73241800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr6:73239600-73242200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr6:73240000-73240600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:73240000-73241800	Enhancers	HMEC	breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links