Variant report

Variant	rs1842759
Chromosome Location	chr5:17059723-17059724
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs11744180	0.87[ASN][1000 genomes]
rs11948837	0.81[ASN][1000 genomes]
rs12186388	0.90[ASN][1000 genomes]
rs12186858	0.90[ASN][1000 genomes]
rs12187047	0.90[ASN][1000 genomes]
rs2086606	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2086608	0.80[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28669748	0.82[ASN][1000 genomes]
rs3860140	0.91[ASN][1000 genomes]
rs4072898	0.90[ASN][1000 genomes]
rs4072899	0.90[ASN][1000 genomes]
rs4607350	0.90[ASN][1000 genomes]
rs4701678	0.88[ASN][1000 genomes]
rs4701680	0.80[ASN][1000 genomes]
rs4702190	0.88[ASN][1000 genomes]
rs4702192	0.90[ASN][1000 genomes]
rs58076264	0.85[ASN][1000 genomes]
rs58236592	0.84[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs58425041	0.90[ASN][1000 genomes]
rs60901893	0.85[ASN][1000 genomes]
rs62348834	0.82[ASN][1000 genomes]
rs62350295	0.86[ASN][1000 genomes]
rs6554964	0.89[ASN][1000 genomes]
rs6554965	0.89[ASN][1000 genomes]
rs6554966	0.91[ASN][1000 genomes]
rs66972346	0.91[EUR][1000 genomes]
rs6862915	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6884918	0.82[ASN][1000 genomes]
rs6890007	0.82[ASN][1000 genomes]
rs6897712	0.91[ASN][1000 genomes]
rs6898175	0.87[ASN][1000 genomes]
rs72636107	0.90[ASN][1000 genomes]
rs72636108	0.90[ASN][1000 genomes]
rs72734394	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7706695	0.85[ASN][1000 genomes]
rs7710867	0.89[ASN][1000 genomes]
rs7723238	0.82[ASN][1000 genomes]
rs7727307	0.85[ASN][1000 genomes]
rs7730952	0.90[ASN][1000 genomes]
rs7737397	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9687340	0.85[ASN][1000 genomes]
rs9688197	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1025225	chr5:16714512-17234866	Enhancers Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv1015247	chr5:16748966-17133274	Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv880277	chr5:16829442-17316288	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
4	esv3510797	chr5:16966764-17125849	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	esv3510798	chr5:16966764-17125849	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	esv1795984	chr5:16973769-17078295	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	nsv1017222	chr5:17001819-17133274	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv1021972	chr5:17011758-17091878	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1026025	chr5:17039665-17195440	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17055600-17060000	Enhancers	Stomach Mucosa	stomach
2	chr5:17056600-17062200	Weak transcription	Placenta	Placenta
3	chr5:17056800-17062200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr5:17056800-17064600	Weak transcription	Ovary	ovary
5	chr5:17058000-17061800	Enhancers	A549	lung
6	chr5:17058200-17061800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr5:17058400-17061800	Weak transcription	Fetal Stomach	stomach
8	chr5:17059200-17060000	Enhancers	Gastric	stomach

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