Variant report

Variant	rs55999326
Chromosome Location	chr8:39930446-39930447
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	chr8:39928502..39931425-chr8:39937811..39939338,2	MCF-7	breast:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs13254619	1.00[ASN][1000 genomes]
rs1481048	1.00[ASN][1000 genomes]
rs1481049	1.00[ASN][1000 genomes]
rs1481052	1.00[ASN][1000 genomes]
rs16888719	1.00[ASN][1000 genomes]
rs16888724	1.00[ASN][1000 genomes]
rs16888726	1.00[ASN][1000 genomes]
rs16888729	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16888732	1.00[ASN][1000 genomes]
rs16888736	1.00[ASN][1000 genomes]
rs16888738	1.00[ASN][1000 genomes]
rs28427344	1.00[ASN][1000 genomes]
rs2981193	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34487659	0.95[ASN][1000 genomes]
rs34852909	1.00[ASN][1000 genomes]
rs4521741	1.00[ASN][1000 genomes]
rs55742726	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55784256	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55956871	0.80[AFR][1000 genomes]
rs55977637	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56302842	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56347116	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57071360	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs57282560	0.90[AMR][1000 genomes]
rs57503829	0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs57560164	0.93[AMR][1000 genomes]
rs57814007	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs58424813	0.93[AMR][1000 genomes]
rs59027887	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59248258	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59404167	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs59885214	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60751747	0.93[AMR][1000 genomes]
rs60772517	1.00[ASN][1000 genomes]
rs61048623	1.00[ASN][1000 genomes]
rs61513602	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61682670	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6474213	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6474215	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6474216	1.00[ASN][1000 genomes]
rs6474217	1.00[ASN][1000 genomes]
rs6983101	1.00[ASN][1000 genomes]
rs6983118	1.00[ASN][1000 genomes]
rs6987482	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6987771	1.00[ASN][1000 genomes]
rs6994138	1.00[ASN][1000 genomes]
rs7000302	0.88[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7000470	1.00[ASN][1000 genomes]
rs7004182	1.00[ASN][1000 genomes]
rs7007403	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7014749	1.00[ASN][1000 genomes]
rs7017503	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7017791	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71510122	1.00[ASN][1000 genomes]
rs71510123	1.00[ASN][1000 genomes]
rs73617874	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73619605	0.97[AMR][1000 genomes]
rs73674750	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7821033	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs7821900	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs7822668	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7822780	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7832286	1.00[ASN][1000 genomes]
rs7836554	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7837003	0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7837122	1.00[ASN][1000 genomes]
rs7837262	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7837573	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7838116	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7838519	1.00[ASN][1000 genomes]
rs7839033	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7841905	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][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	nsv539555	chr8:39683857-40673606	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv534582	chr8:39884590-40653224	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39913000-39939000	Weak transcription	Right Atrium	heart
2	chr8:39928600-39932000	Weak transcription	A549	lung
3	chr8:39929400-39932400	Weak transcription	Fetal Intestine Small	intestine
4	chr8:39930000-39937800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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