Variant report

Variant	rs1544145
Chromosome Location	chr6:86740845-86740846
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs12193987	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1337852	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1337853	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1413727	1.00[EUR][1000 genomes]
rs1413728	1.00[EUR][1000 genomes]
rs1415752	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1415755	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1544146	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1577918	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16876674	1.00[EUR][1000 genomes]
rs16876678	1.00[EUR][1000 genomes]
rs16876681	1.00[EUR][1000 genomes]
rs1933157	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1960942	1.00[EUR][1000 genomes]
rs2174772	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2206976	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2782260	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2812969	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2816813	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4441929	1.00[EUR][1000 genomes]
rs58373384	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60365088	1.00[EUR][1000 genomes]
rs6454514	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6909369	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6910480	1.00[EUR][1000 genomes]
rs6910486	1.00[EUR][1000 genomes]
rs6915507	0.90[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs700511	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72493076	1.00[EUR][1000 genomes]
rs7741714	1.00[EUR][1000 genomes]
rs7743257	1.00[EUR][1000 genomes]
rs7753603	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7773476	1.00[EUR][1000 genomes]
rs7773518	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791853	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791854	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791855	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791857	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9353354	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][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	nsv1028293	chr6:86353958-86778912	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
2	nsv538350	chr6:86353958-86778912	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	100 gene(s)	inside rSNPs	diseases
3	nsv1022618	chr6:86465365-87432069	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv538352	chr6:86465365-87432069	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1018453	chr6:86555984-86761120	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1021292	chr6:86611922-86778912	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv508420	chr6:86701551-86751873	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:86739600-86741600	Weak transcription	Fetal Lung	lung
2	chr6:86740200-86742200	Enhancers	Liver	Liver
3	chr6:86740600-86741000	Enhancers	HepG2	liver
4	chr6:86740800-86742000	Enhancers	Stomach Smooth Muscle	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links