Variant report

Variant	rs61770408
Chromosome Location	chr1:85233850-85233851
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs1077776	1.00[ASN][1000 genomes]
rs1077777	1.00[ASN][1000 genomes]
rs1325274	1.00[ASN][1000 genomes]
rs1417296	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1417297	1.00[ASN][1000 genomes]
rs1417299	1.00[ASN][1000 genomes]
rs17115425	1.00[ASN][1000 genomes]
rs17115551	1.00[ASN][1000 genomes]
rs17115615	1.00[ASN][1000 genomes]
rs17116652	1.00[ASN][1000 genomes]
rs17368823	1.00[ASN][1000 genomes]
rs17377380	1.00[ASN][1000 genomes]
rs2025689	1.00[ASN][1000 genomes]
rs2389776	1.00[ASN][1000 genomes]
rs2389777	1.00[ASN][1000 genomes]
rs2389785	1.00[ASN][1000 genomes]
rs4484942	1.00[ASN][1000 genomes]
rs4907094	1.00[ASN][1000 genomes]
rs4907100	1.00[ASN][1000 genomes]
rs55852981	1.00[ASN][1000 genomes]
rs57744031	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57925971	1.00[ASN][1000 genomes]
rs58803630	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59493945	1.00[ASN][1000 genomes]
rs59536255	1.00[ASN][1000 genomes]
rs61768760	1.00[ASN][1000 genomes]
rs61770401	1.00[ASN][1000 genomes]
rs61770406	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61770411	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61770414	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61770417	1.00[ASN][1000 genomes]
rs61770418	1.00[ASN][1000 genomes]
rs61770419	1.00[ASN][1000 genomes]
rs61770433	1.00[ASN][1000 genomes]
rs61770434	1.00[ASN][1000 genomes]
rs61770435	1.00[ASN][1000 genomes]
rs61770436	1.00[ASN][1000 genomes]
rs61770437	1.00[ASN][1000 genomes]
rs61770439	1.00[ASN][1000 genomes]
rs61770440	1.00[ASN][1000 genomes]
rs61770441	1.00[ASN][1000 genomes]
rs61770442	1.00[ASN][1000 genomes]
rs61770443	1.00[ASN][1000 genomes]
rs61770444	1.00[ASN][1000 genomes]
rs61770446	1.00[ASN][1000 genomes]
rs72718785	1.00[ASN][1000 genomes]
rs72942437	1.00[ASN][1000 genomes]
rs9659298	1.00[ASN][1000 genomes]
rs9660220	1.00[ASN][1000 genomes]
rs9660249	1.00[ASN][1000 genomes]
rs9661368	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9661377	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9661394	1.00[ASN][1000 genomes]
rs9728153	1.00[ASN][1000 genomes]
rs9728717	1.00[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	nsv947190	chr1:85229432-85235799	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85228800-85238200	Weak transcription	Stomach Mucosa	stomach
2	chr1:85230600-85234400	Weak transcription	Fetal Brain Male	brain
3	chr1:85231400-85240400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:85232600-85237800	Weak transcription	Fetal Heart	heart
5	chr1:85233600-85234200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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