Variant report

Variant	rs10485210
Chromosome Location	chr6:73234957-73234958
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10085254	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10485211	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1147534	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1147536	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1147537	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1147538	0.90[EUR][1000 genomes]
rs1147540	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1147569	1.00[GIH][hapmap]
rs1202107	1.00[CEU][hapmap]
rs1202110	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1202117	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1202118	0.90[EUR][1000 genomes]
rs1202120	0.90[EUR][1000 genomes]
rs1202121	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1202122	0.90[EUR][1000 genomes]
rs1334345	0.92[EUR][1000 genomes]
rs1590801	1.00[CEU][hapmap];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs16882468	0.96[EUR][1000 genomes]
rs16882473	1.00[EUR][1000 genomes]
rs16882476	0.98[EUR][1000 genomes]
rs16882487	1.00[CEU][hapmap]
rs16882500	1.00[CEU][hapmap]
rs16882506	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16882539	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4307137	1.00[EUR][1000 genomes]
rs55739455	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59106883	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs59352656	1.00[EUR][1000 genomes]
rs61032405	1.00[EUR][1000 genomes]
rs66805874	0.90[EUR][1000 genomes]
rs68186765	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6909267	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72939319	0.96[EUR][1000 genomes]
rs72941783	0.92[EUR][1000 genomes]
rs72941788	0.92[EUR][1000 genomes]
rs72943183	1.00[EUR][1000 genomes]
rs72946182	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72946193	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72948113	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9442816	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9442819	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9446697	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9446701	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9446703	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9446704	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9446705	0.82[AMR][1000 genomes];0.84[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:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73232800-73243000	Weak transcription	K562	blood
2	chr6:73234000-73235000	Weak transcription	HSMMtube	muscle
3	chr6:73234200-73235200	Weak transcription	HSMM	muscle
4	chr6:73234200-73239600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr6:73234200-73240000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:73234400-73239600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:73234400-73239600	Weak transcription	NHEK	skin

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