Variant report

Variant	rs722969
Chromosome Location	chr10:25938940-25938941
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOXA1	chr10:25938674-25939050	T-47D	breast:	n/a	chr10:25938857-25938869

Variant related genes	Relation type
GPN3P1	TF binding region

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs11014622	1.00[ASN][1000 genomes]
rs11014623	1.00[ASN][1000 genomes]
rs11014625	1.00[ASN][1000 genomes]
rs12355530	1.00[ASN][1000 genomes]
rs12357174	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1329254	1.00[ASN][1000 genomes]
rs1335195	1.00[CHB][hapmap]
rs1335196	1.00[CHB][hapmap]
rs1335197	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs1360124	1.00[ASN][1000 genomes]
rs1547685	1.00[ASN][1000 genomes]
rs16926124	1.00[CHB][hapmap]
rs16926153	1.00[CHB][hapmap]
rs16926172	1.00[CHB][hapmap]
rs17557337	1.00[ASN][1000 genomes]
rs17557638	1.00[ASN][1000 genomes]
rs1773635	1.00[ASN][1000 genomes]
rs17737176	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17737261	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1928364	1.00[ASN][1000 genomes]
rs1999111	1.00[ASN][1000 genomes]
rs2437383	1.00[CHB][hapmap]
rs2480346	1.00[ASN][1000 genomes]
rs2505429	1.00[CHB][hapmap]
rs2987837	1.00[ASN][1000 genomes]
rs3005186	1.00[ASN][1000 genomes]
rs3005188	1.00[ASN][1000 genomes]
rs3005190	1.00[ASN][1000 genomes]
rs3005192	1.00[ASN][1000 genomes]
rs3118971	1.00[ASN][1000 genomes]
rs34567803	1.00[ASN][1000 genomes]
rs4237372	1.00[ASN][1000 genomes]
rs4237374	1.00[ASN][1000 genomes]
rs4523593	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4747532	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs4747533	1.00[ASN][1000 genomes]
rs4749050	1.00[ASN][1000 genomes]
rs55945306	0.86[AFR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56386940	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58949541	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59190298	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61846881	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61846905	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6482497	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6482498	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs6482499	1.00[CHB][hapmap]
rs702979	1.00[ASN][1000 genomes]
rs7070879	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7091731	1.00[ASN][1000 genomes]
rs7094086	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7095138	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7099100	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7906914	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7911892	1.00[CHB][hapmap]
rs7921299	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs824606	1.00[ASN][1000 genomes]
rs824611	1.00[ASN][1000 genomes]
rs866089	1.00[ASN][1000 genomes]
rs866869	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	esv3349863	chr10:25614571-25946379	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1044482	chr10:25889919-25977270	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 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
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