Variant report

Variant	rs60150269
Chromosome Location	chr12:66857862-66857863
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11176256	1.00[AMR][1000 genomes]
rs11176257	1.00[AMR][1000 genomes]
rs11176295	1.00[AMR][1000 genomes]
rs11176296	1.00[AMR][1000 genomes]
rs11504204	1.00[AMR][1000 genomes]
rs12297649	1.00[AMR][1000 genomes]
rs12309622	1.00[AMR][1000 genomes]
rs12309778	1.00[AMR][1000 genomes]
rs12309896	1.00[AMR][1000 genomes]
rs12311664	1.00[AMR][1000 genomes]
rs12313212	1.00[AMR][1000 genomes]
rs12319060	1.00[AMR][1000 genomes]
rs12319603	1.00[AMR][1000 genomes]
rs12321077	1.00[AMR][1000 genomes]
rs12321492	1.00[AMR][1000 genomes]
rs12321495	1.00[AMR][1000 genomes]
rs12321549	1.00[AMR][1000 genomes]
rs13377630	1.00[AMR][1000 genomes]
rs13377875	1.00[AMR][1000 genomes]
rs13378006	1.00[AMR][1000 genomes]
rs17102568	1.00[AMR][1000 genomes]
rs17102569	1.00[AMR][1000 genomes]
rs1813738	1.00[AMR][1000 genomes]
rs1908122	1.00[AMR][1000 genomes]
rs2009924	1.00[AMR][1000 genomes]
rs57630867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58011515	1.00[AMR][1000 genomes]
rs58314154	1.00[AMR][1000 genomes]
rs58520471	1.00[AMR][1000 genomes]
rs59000682	1.00[AMR][1000 genomes]
rs59253853	1.00[AMR][1000 genomes]
rs60436125	1.00[AMR][1000 genomes]
rs60605218	1.00[AMR][1000 genomes]
rs60935597	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61448698	1.00[AMR][1000 genomes]
rs7974745	1.00[AMR][1000 genomes]
rs7974896	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1051713	chr12:66745716-66889411	Strong transcription Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1040682	chr12:66750103-67328053	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv832447	chr12:66785814-66990029	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv469459	chr12:66854354-66950289	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv559206	chr12:66854354-66950289	Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:66823200-66859000	Weak transcription	Brain Germinal Matrix	brain
2	chr12:66838800-66858400	Weak transcription	Fetal Brain Female	brain
3	chr12:66844000-66861600	Weak transcription	Primary T cells from cord blood	blood
4	chr12:66846800-66860200	Weak transcription	Colon Smooth Muscle	Colon
5	chr12:66849400-66866400	Weak transcription	Pancreas	Pancrea
6	chr12:66849600-66860000	Weak transcription	Esophagus	oesophagus
7	chr12:66853000-66876200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:66856800-66859600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr12:66856800-66868400	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr12:66857600-66858000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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