Variant report

Variant	rs10172384
Chromosome Location	chr2:178656022-178656023
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10178473	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10178858	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10178916	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10179500	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10182017	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10182353	0.84[AFR][1000 genomes];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10185318	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13395965	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13396065	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13396537	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13421345	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1438042	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs28380215	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4297923	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4464321	0.86[AFR][1000 genomes]
rs56314683	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs56690966	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs57342997	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6433694	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6709966	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6718100	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6718657	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6718993	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6726253	0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6726502	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6733980	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6737872	0.81[EUR][1000 genomes]
rs6743821	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6747512	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6751656	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6752264	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6758508	0.85[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7563242	0.82[EUR][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	nsv583690	chr2:178638381-178712283	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:178649400-178662000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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