Variant report

Variant	rs7741026
Chromosome Location	chr6:25642712-25642713
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 47 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10456322	1.00[JPT][hapmap]
rs10456323	1.00[JPT][hapmap]
rs10456325	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12191432	1.00[JPT][hapmap]
rs12192331	1.00[JPT][hapmap]
rs12192342	0.85[GIH][hapmap];1.00[JPT][hapmap]
rs12195457	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs12201249	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12207791	1.00[JPT][hapmap]
rs12208868	1.00[JPT][hapmap]
rs12216281	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1410443	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs150533	1.00[JPT][hapmap]
rs184202	1.00[JPT][hapmap]
rs1883257	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1884575	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs212927	1.00[JPT][hapmap]
rs212929	0.89[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs212931	1.00[JPT][hapmap]
rs212932	1.00[JPT][hapmap]
rs212935	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs212937	1.00[JPT][hapmap]
rs212939	0.89[CEU][hapmap];1.00[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs212940	1.00[JPT][hapmap]
rs301377	1.00[JPT][hapmap]
rs441472	1.00[JPT][hapmap]
rs453181	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs485567	1.00[JPT][hapmap]
rs6902158	1.00[JPT][hapmap]
rs6913169	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6918563	0.87[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6927384	1.00[JPT][hapmap]
rs6931843	1.00[JPT][hapmap]
rs72840515	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72840523	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72840524	0.88[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs72840525	0.92[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7742338	1.00[JPT][hapmap]
rs9348685	0.81[GIH][hapmap];1.00[JPT][hapmap]
rs9379774	1.00[JPT][hapmap]
rs9461190	0.89[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.83[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9467544	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9467555	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883488	chr6:25592489-25731691	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
4	nsv427747	chr6:25641380-25908218	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs7741026	ZNF391	cis	parietal	SCAN
rs7741026	LRRC16	cis	lesional skin	skin_eQTL
rs7741026	SCGN	cis	Liver	GTEx
rs7741026	SCGN	cis	multi-tissue	Pritchard
rs7741026	BTN1A1	cis	cerebellum	SCAN
rs7741026	ZNF187	cis	parietal	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:25641200-25651800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:25641800-25644000	Enhancers	Brain Germinal Matrix	brain
3	chr6:25642000-25643800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr6:25642400-25642800	Active TSS	A549	lung
5	chr6:25642400-25643200	Enhancers	Fetal Kidney	kidney
6	chr6:25642600-25642800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr6:25642600-25642800	Enhancers	HepG2	liver

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