Variant report

Variant	rs13159764
Chromosome Location	chr5:49940840-49940841
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 59 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10041633	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10045122	0.83[AMR][1000 genomes]
rs10052001	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10071272	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10434558	0.81[EUR][1000 genomes]
rs10471940	0.82[AFR][1000 genomes]
rs10940423	0.85[EUR][1000 genomes]
rs10940424	0.91[EUR][1000 genomes]
rs11738761	0.91[EUR][1000 genomes]
rs11741205	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11745945	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12653803	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs13162921	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1839128	0.91[EUR][1000 genomes]
rs1900738	0.91[EUR][1000 genomes]
rs1972980	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1988613	0.82[AFR][1000 genomes]
rs2034392	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2034393	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2034394	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2121979	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2166893	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2166894	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4101529	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4282859	0.91[EUR][1000 genomes]
rs4415044	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4440312	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4865846	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4865895	0.91[EUR][1000 genomes]
rs4865896	0.87[EUR][1000 genomes]
rs6450292	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6863575	0.87[EUR][1000 genomes]
rs6867590	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6872070	0.91[EUR][1000 genomes]
rs6879306	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6888147	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7702541	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7709831	0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7710150	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7711839	0.82[AFR][1000 genomes]
rs7721050	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7728222	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7730847	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7736142	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016583	chr5:49455624-50116720	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv1023140	chr5:49455624-50121623	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1022067	chr5:49584188-49960083	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv537758	chr5:49584188-49960083	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv918220	chr5:49584188-50111282	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv931010	chr5:49584189-50118254	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv523212	chr5:49597497-50058043	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	esv2757995	chr5:49748352-50058182	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	esv2759342	chr5:49748352-50058182	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	nsv964850	chr5:49883635-49942856	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv16870	chr5:49885849-49989415	Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv965011	chr5:49934158-49942856	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	inside rSNPs	diseases
13	nsv980790	chr5:49934158-49945480	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	n/a	n/a	inside rSNPs	diseases
14	esv3327506	chr5:49940145-49943093	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
15	esv3323632	chr5:49940545-49942893	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13159764	LOC647121	Cis_1M	lymphoblastoid	RTeQTL
rs13159764	PARP8	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:49933800-49942400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chr5:49934200-49943800	Weak transcription	Primary T helper cells PMA-I stimulated	--
3	chr5:49939200-49942400	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr5:49939400-49942400	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr5:49939400-49942400	Weak transcription	Monocytes-CD14+_RO01746	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links