Variant report

Variant	rs12538071
Chromosome Location	chr7:137894519-137894520
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs1074096	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12531545	0.86[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12536908	0.80[AMR][1000 genomes]
rs12538075	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12540428	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs1602106	0.86[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs2087468	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs4142643	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs56250738	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs57484232	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs57501836	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs60045404	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs60139929	0.89[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs61272163	0.86[ASN][1000 genomes]
rs6467747	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs6967735	0.85[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73452738	0.85[AMR][1000 genomes]
rs73452748	0.92[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs73452751	0.91[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs73452757	0.88[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs73456792	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs73458710	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs73458718	0.83[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs7777620	0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs7787920	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7803515	0.88[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7806331	0.89[AMR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137892000-137895400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:137893200-137894600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr7:137893200-137894600	Enhancers	Pancreas	Pancrea
4	chr7:137893600-137894600	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
5	chr7:137893800-137905200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr7:137894000-137895000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
7	chr7:137894000-137895800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr7:137894000-137896800	Weak transcription	HepG2	liver
9	chr7:137894200-137894600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:137894200-137895400	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
11	chr7:137894200-137902400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr7:137894400-137894800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
13	chr7:137894400-137896800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr7:137894400-137897000	Weak transcription	Liver	Liver
15	chr7:137894400-137899400	Weak transcription	H1 Cell Line	embryonic stem cell

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