Variant report

Variant	rs10956181
Chromosome Location	chr8:125430997-125430998
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:125384917..125387292-chr8:125428430..125431299,2	MCF-7	breast:
2	chr8:125430987..125433174-chr8:125436627..125439143,3	MCF-7	breast:
3	chr8:125429633..125432443-chr8:125437672..125439432,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164983	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10086126	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10091131	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10103889	0.81[AMR][1000 genomes]
rs10103942	0.81[AMR][1000 genomes]
rs10103986	0.81[AMR][1000 genomes]
rs10104258	0.81[AMR][1000 genomes]
rs10111265	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10111274	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs10111582	0.91[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs10111705	0.81[AMR][1000 genomes]
rs10956179	0.81[AMR][1000 genomes]
rs10956180	0.81[AMR][1000 genomes]
rs11991060	0.87[AFR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11993622	0.81[AMR][1000 genomes]
rs12677019	0.91[EUR][1000 genomes]
rs13266094	0.86[EUR][1000 genomes]
rs13269278	0.83[EUR][1000 genomes]
rs13277120	0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4346978	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4376484	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4425736	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4487744	0.81[EUR][1000 genomes]
rs6993890	0.81[AMR][1000 genomes]
rs6994603	0.81[AMR][1000 genomes]
rs7839446	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9643194	0.81[AMR][1000 genomes]
rs9643196	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2762769	chr8:125167256-125480574	Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1034768	chr8:125323011-125481733	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv527751	chr8:125338216-125431030	Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
4	nsv531508	chr8:125390194-125587953	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
5	esv275091	chr8:125430760-125437615	Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125427200-125433800	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr8:125430400-125431000	Enhancers	Fetal Heart	heart
3	chr8:125430600-125437800	Weak transcription	Left Ventricle	heart

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