Variant report

Variant	rs12037077
Chromosome Location	chr1:79350364-79350365
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11162565	0.84[ASN][1000 genomes]
rs12026347	0.87[ASN][1000 genomes]
rs12037897	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12401934	0.87[ASN][1000 genomes]
rs1248483	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1489398	0.98[ASN][1000 genomes]
rs1532102	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1552571	0.95[ASN][1000 genomes]
rs1552572	0.95[ASN][1000 genomes]
rs1552573	0.95[ASN][1000 genomes]
rs1632786	0.93[ASN][1000 genomes]
rs1686340	0.95[ASN][1000 genomes]
rs1686342	0.98[ASN][1000 genomes]
rs17411879	0.87[ASW][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes]
rs1780709	0.97[ASN][1000 genomes]
rs1780731	0.95[ASN][1000 genomes]
rs1937016	0.91[ASN][1000 genomes]
rs1968952	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1968953	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1968954	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2054927	0.98[ASN][1000 genomes]
rs2352520	0.88[ASN][1000 genomes]
rs2801027	0.95[ASN][1000 genomes]
rs28813447	0.94[ASN][1000 genomes]
rs2932176	0.96[ASN][1000 genomes]
rs2932177	0.88[ASN][1000 genomes]
rs2996691	0.95[ASN][1000 genomes]
rs2996693	0.88[ASN][1000 genomes]
rs2996694	0.87[ASN][1000 genomes]
rs3012079	0.95[ASN][1000 genomes]
rs3012080	0.97[ASN][1000 genomes]
rs3012084	0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4284216	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4515744	0.86[ASN][1000 genomes]
rs6680564	0.87[ASN][1000 genomes]
rs6694893	0.87[ASN][1000 genomes]
rs7355057	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv871835	chr1:78528803-79501129	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv491784	chr1:79146141-79853482	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv526221	chr1:79197624-79487080	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv817535	chr1:79203834-79473089	Enhancers Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv999624	chr1:79230028-79448222	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv535013	chr1:79230028-79448222	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv546619	chr1:79233493-79614989	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	esv2830430	chr1:79310760-79555593	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1010441	chr1:79320299-79555315	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv871700	chr1:79325216-79350364	Enhancers Weak transcription ZNF genes & repeats	lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:79346400-79350800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr1:79346600-79350800	Weak transcription	HUVEC	blood vessel
3	chr1:79348600-79405600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:79350200-79350400	Enhancers	Hela-S3	cervix
5	chr1:79350200-79350600	Enhancers	Colon Smooth Muscle	Colon
6	chr1:79350200-79351000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr1:79350200-79351000	Enhancers	Rectal Smooth Muscle	rectum
8	chr1:79350200-79351200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:79350200-79351200	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr1:79350200-79351400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:79350200-79351400	Enhancers	iPS-18 Cell Line	embryonic stem cell

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