Variant report

Variant	rs67597785
Chromosome Location	chr6:99399037-99399038
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:99397150..99399424-chr6:99402410..99404816,2	K562	blood:
2	chr6:99395967..99397726-chr6:99398080..99400447,2	MCF-7	breast:
3	chr6:99394294..99397680-chr6:99397725..99402132,5	K562	blood:

Variant related genes	Relation type
ENSG00000112234	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10484609	0.92[ASN][1000 genomes]
rs12110362	0.92[ASN][1000 genomes]
rs12110701	0.92[ASN][1000 genomes]
rs12110702	0.92[ASN][1000 genomes]
rs13194064	0.92[ASN][1000 genomes]
rs13217727	0.92[ASN][1000 genomes]
rs1884185	0.81[AFR][1000 genomes]
rs195842	0.96[ASN][1000 genomes]
rs2016597	0.81[AFR][1000 genomes]
rs2124137	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2267924	0.92[ASN][1000 genomes]
rs2281123	0.92[ASN][1000 genomes]
rs2300060	0.92[ASN][1000 genomes]
rs2300062	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2300063	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs28488166	0.81[AFR][1000 genomes]
rs3756986	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs3765239	0.92[ASN][1000 genomes]
rs3811071	0.90[ASN][1000 genomes]
rs3823035	0.92[ASN][1000 genomes]
rs4407721	0.89[ASN][1000 genomes]
rs6921694	0.88[ASN][1000 genomes]
rs6924301	0.81[AFR][1000 genomes]
rs6928645	0.84[AFR][1000 genomes]
rs6929427	0.92[ASN][1000 genomes]
rs73505759	0.84[AFR][1000 genomes]
rs760765	0.89[ASN][1000 genomes]
rs760766	0.89[ASN][1000 genomes]
rs7742800	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7759571	0.80[ASN][1000 genomes]
rs9321243	0.92[ASN][1000 genomes]
rs9372960	0.81[AFR][1000 genomes]
rs9372982	0.84[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs9372983	0.84[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs9375713	0.92[ASN][1000 genomes]
rs9375721	0.84[AFR][1000 genomes]
rs9375728	0.92[ASN][1000 genomes]
rs9375729	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9375730	0.92[ASN][1000 genomes]
rs9375733	0.92[ASN][1000 genomes]
rs9375750	0.90[ASN][1000 genomes]
rs9375807	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9385541	0.90[ASN][1000 genomes]
rs9385544	0.84[AFR][1000 genomes]
rs9388788	0.92[ASN][1000 genomes]
rs9388789	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9388809	0.91[ASN][1000 genomes]
rs9388815	0.92[ASN][1000 genomes]
rs9388899	0.84[AFR][1000 genomes]
rs9402227	0.90[ASN][1000 genomes]
rs9402228	0.92[ASN][1000 genomes]
rs9402235	0.92[ASN][1000 genomes]
rs9402255	0.92[ASN][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	nsv604253	chr6:98857397-99630038	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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