Variant report

Variant	rs7798039
Chromosome Location	chr7:79919100-79919101
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10081383	0.99[ASN][1000 genomes]
rs10215570	0.86[ASN][1000 genomes]
rs10224409	0.86[ASN][1000 genomes]
rs10226374	0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10235376	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10245039	0.95[ASN][1000 genomes]
rs10246790	0.89[ASN][1000 genomes]
rs10249625	0.99[ASN][1000 genomes]
rs10269645	0.86[ASN][1000 genomes]
rs10954137	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13222182	0.96[ASN][1000 genomes]
rs13226877	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13229096	0.90[ASN][1000 genomes]
rs13230620	0.88[ASN][1000 genomes]
rs13233772	0.98[ASN][1000 genomes]
rs13234088	1.00[ASN][1000 genomes]
rs13237208	0.97[ASN][1000 genomes]
rs13237302	1.00[ASN][1000 genomes]
rs13237312	1.00[ASN][1000 genomes]
rs13238619	0.91[ASN][1000 genomes]
rs13243724	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1995971	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2048474	0.97[ASN][1000 genomes]
rs2158123	0.97[ASN][1000 genomes]
rs28584961	0.90[ASN][1000 genomes]
rs28875814	0.86[ASN][1000 genomes]
rs3914181	0.86[ASN][1000 genomes]
rs4731329	0.95[EUR][1000 genomes]
rs4731336	0.85[EUR][1000 genomes]
rs67417372	0.97[ASN][1000 genomes]
rs7782930	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7785183	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7797587	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9656355	0.97[ASN][1000 genomes]
rs979425	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1024312	chr7:79832637-80004812	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv1029180	chr7:79832637-80017560	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	esv2761340	chr7:79905897-79922486	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:79913400-79922000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:79914800-79923400	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr7:79915000-79923600	Weak transcription	NHLF	lung
4	chr7:79917800-79923200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr7:79917800-79923200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr7:79918600-79923400	Weak transcription	Osteobl	bone

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