Variant report

Variant	rs7862197
Chromosome Location	chr9:102204754-102204755
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1025901	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1025902	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10441760	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10441761	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10760684	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10760685	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10819666	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10819667	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10819672	0.89[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10819674	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10988816	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10988829	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12238127	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1360260	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1530379	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1972233	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2416768	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4743345	0.84[ASN][1000 genomes]
rs4743347	0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4743348	0.84[ASN][1000 genomes]
rs4743349	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4743353	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55750347	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs57483311	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7027953	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7032399	0.81[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7032541	0.84[ASN][1000 genomes]
rs7040144	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73495500	0.84[ASN][1000 genomes]
rs7847405	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7857445	0.84[ASN][1000 genomes]
rs7858078	0.80[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7866560	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs878449	0.84[ASN][1000 genomes]
rs880597	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831667	chr9:102068047-102285691	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv527165	chr9:102194921-102214169	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv6636	chr9:102197504-102242604	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	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	chr9:102197000-102207600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr9:102201000-102207000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr9:102202800-102206600	Weak transcription	NHDF-Ad	bronchial

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