Variant report

Variant	rs61425825
Chromosome Location	chr2:178513722-178513723
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:178504624..178506864-chr2:178511497..178514484,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10497494	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497495	0.91[ASN][1000 genomes]
rs1106074	0.91[ASN][1000 genomes]
rs1527405	0.87[ASN][1000 genomes]
rs1527408	0.87[ASN][1000 genomes]
rs16865452	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16865453	0.85[ASN][1000 genomes]
rs16865475	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs16865492	0.86[ASN][1000 genomes]
rs16865501	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16865508	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16865509	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16865514	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16865524	0.91[ASN][1000 genomes]
rs2178018	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2293472	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2293473	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2365618	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3731803	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3731806	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3821005	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4144277	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5025339	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57000468	0.91[ASN][1000 genomes]
rs57401542	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57479066	0.91[ASN][1000 genomes]
rs57595473	1.00[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs58970701	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59275027	0.91[ASN][1000 genomes]
rs59963196	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60941291	0.91[ASN][1000 genomes]
rs61311927	0.86[ASN][1000 genomes]
rs61457959	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61570618	1.00[ASN][1000 genomes]
rs6745743	0.91[ASN][1000 genomes]
rs6746845	0.83[ASN][1000 genomes]
rs73977682	0.91[ASN][1000 genomes]
rs73977683	0.91[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	nsv999086	chr2:178262348-178773585	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv536055	chr2:178262348-178773585	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv583688	chr2:178427640-178540293	Enhancers Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178509000-178516600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:178512000-178516400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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