Variant report

Variant	rs13167690
Chromosome Location	chr5:43154562-43154563
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:43120824..43123144-chr5:43153299..43156579,5	MCF-7	breast:
2	chr5:43142089..43145048-chr5:43154382..43156409,2	K562	blood:
3	chr5:43134921..43137750-chr5:43153839..43155505,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000172262	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:100)

rs_ID	r²[population]
rs1001717	0.99[EUR][1000 genomes]
rs12657208	0.88[EUR][1000 genomes]
rs13153077	0.94[EUR][1000 genomes]
rs13153860	0.94[EUR][1000 genomes]
rs13154654	0.95[EUR][1000 genomes]
rs13158800	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13159390	0.99[EUR][1000 genomes]
rs13161127	1.00[EUR][1000 genomes]
rs13163892	0.94[EUR][1000 genomes]
rs13164183	0.94[EUR][1000 genomes]
rs13166780	1.00[EUR][1000 genomes]
rs13167375	0.81[EUR][1000 genomes]
rs13171192	0.82[EUR][1000 genomes]
rs13171253	1.00[EUR][1000 genomes]
rs13172378	1.00[EUR][1000 genomes]
rs13174772	0.99[EUR][1000 genomes]
rs13178478	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13181290	1.00[EUR][1000 genomes]
rs13182652	0.82[EUR][1000 genomes]
rs13186091	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs13186549	0.91[EUR][1000 genomes]
rs13189565	0.91[EUR][1000 genomes]
rs13189574	1.00[EUR][1000 genomes]
rs13190109	0.94[EUR][1000 genomes]
rs16873177	1.00[EUR][1000 genomes]
rs17242731	0.99[EUR][1000 genomes]
rs17242995	1.00[EUR][1000 genomes]
rs17243023	1.00[EUR][1000 genomes]
rs17243086	1.00[EUR][1000 genomes]
rs17243165	0.94[EUR][1000 genomes]
rs17243515	0.91[EUR][1000 genomes]
rs17302596	1.00[EUR][1000 genomes]
rs17302931	0.90[EUR][1000 genomes]
rs2005510	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28548198	0.99[EUR][1000 genomes]
rs34071473	1.00[EUR][1000 genomes]
rs34205479	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34242142	0.94[EUR][1000 genomes]
rs34258100	0.94[EUR][1000 genomes]
rs34302880	0.97[EUR][1000 genomes]
rs34333393	1.00[EUR][1000 genomes]
rs34375419	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34448278	0.94[EUR][1000 genomes]
rs34517361	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs34552214	1.00[EUR][1000 genomes]
rs34973629	1.00[EUR][1000 genomes]
rs34992478	1.00[EUR][1000 genomes]
rs35018789	1.00[EUR][1000 genomes]
rs35106307	0.94[EUR][1000 genomes]
rs35199583	0.99[EUR][1000 genomes]
rs35230086	1.00[EUR][1000 genomes]
rs35285338	0.94[EUR][1000 genomes]
rs35321959	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35397154	0.94[EUR][1000 genomes]
rs35484826	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35593061	0.87[EUR][1000 genomes]
rs35645372	0.94[EUR][1000 genomes]
rs35665483	0.99[EUR][1000 genomes]
rs35673052	0.94[EUR][1000 genomes]
rs35754881	0.99[EUR][1000 genomes]
rs35759340	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35837951	1.00[ASN][1000 genomes]
rs35839054	0.91[EUR][1000 genomes]
rs35855029	0.94[EUR][1000 genomes]
rs35859204	0.91[EUR][1000 genomes]
rs35949944	0.97[EUR][1000 genomes]
rs35998500	1.00[EUR][1000 genomes]
rs36054188	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36106080	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs36122541	1.00[EUR][1000 genomes]
rs36125638	0.92[EUR][1000 genomes]
rs3752831	0.94[EUR][1000 genomes]
rs3752832	0.94[EUR][1000 genomes]
rs3797306	0.99[EUR][1000 genomes]
rs3797307	0.99[EUR][1000 genomes]
rs3797308	0.99[EUR][1000 genomes]
rs3797309	0.99[EUR][1000 genomes]
rs56889091	0.94[EUR][1000 genomes]
rs56923657	0.99[EUR][1000 genomes]
rs58028166	0.91[EUR][1000 genomes]
rs67190423	1.00[EUR][1000 genomes]
rs67596313	0.99[EUR][1000 genomes]
rs67756718	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71590635	1.00[EUR][1000 genomes]
rs71627575	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71627578	0.97[EUR][1000 genomes]
rs71627579	1.00[EUR][1000 genomes]
rs71627580	1.00[EUR][1000 genomes]
rs71627583	0.99[EUR][1000 genomes]
rs71627584	1.00[EUR][1000 genomes]
rs71627585	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs71627586	0.94[EUR][1000 genomes]
rs71627587	0.90[EUR][1000 genomes]
rs72748883	0.99[EUR][1000 genomes]
rs72748886	0.90[EUR][1000 genomes]
rs72748897	0.99[EUR][1000 genomes]
rs72750704	0.99[EUR][1000 genomes]
rs72750764	0.99[EUR][1000 genomes]
rs72750780	1.00[EUR][1000 genomes]
rs878234	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
5	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv1024636	chr5:42959979-43295782	Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
7	nsv537739	chr5:42959979-43295782	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	283 gene(s)	inside rSNPs	diseases
8	nsv830274	chr5:43095551-43226087	Strong transcription Transcr. at gene 5' and 3' Genic enhancers Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	138 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13167690	ZNF131	Cis_1M	lymphoblastoid	RTeQTL
rs13167690	ZNF131	cis	Artery Tibial	GTEx

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:43122600-43156200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:43122600-43163400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr5:43122800-43154600	Weak transcription	Aorta	Aorta
4	chr5:43122800-43156400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr5:43122800-43174200	Weak transcription	Colonic Mucosa	Colon
6	chr5:43124000-43183000	Weak transcription	Small Intestine	intestine
7	chr5:43124400-43154600	Weak transcription	Fetal Heart	heart
8	chr5:43124400-43154800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr5:43126600-43154800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr5:43127600-43178000	Strong transcription	Dnd41	blood
11	chr5:43128000-43154600	Weak transcription	Brain Substantia Nigra	brain
12	chr5:43128200-43156000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr5:43128200-43161000	Weak transcription	Rectal Smooth Muscle	rectum
14	chr5:43128400-43154600	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr5:43128400-43161400	Weak transcription	HSMMtube	muscle
16	chr5:43128600-43155400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr5:43129000-43161400	Weak transcription	Colon Smooth Muscle	Colon
18	chr5:43130200-43156200	Weak transcription	Gastric	stomach
19	chr5:43131000-43159800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
20	chr5:43133000-43161400	Weak transcription	Esophagus	oesophagus
21	chr5:43133200-43161400	Weak transcription	Fetal Brain Male	brain
22	chr5:43134000-43154600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr5:43134600-43155000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr5:43135400-43156400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr5:43137200-43163400	Weak transcription	Fetal Kidney	kidney
26	chr5:43137800-43161000	Weak transcription	HSMM	muscle
27	chr5:43138200-43159000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr5:43140400-43154600	Weak transcription	Brain Angular Gyrus	brain
29	chr5:43140400-43155400	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr5:43140600-43154600	Weak transcription	Brain Anterior Caudate	brain
31	chr5:43140800-43155200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr5:43140800-43155800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr5:43141800-43154600	Weak transcription	Left Ventricle	heart
34	chr5:43141800-43161400	Weak transcription	HUVEC	blood vessel
35	chr5:43142200-43161400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr5:43143000-43161400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr5:43143400-43178200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr5:43143800-43155600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr5:43143800-43161400	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr5:43143800-43161400	Weak transcription	NHEK	skin
41	chr5:43144600-43159600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr5:43145200-43161400	Weak transcription	NH-A	brain
43	chr5:43145400-43155400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
44	chr5:43145400-43156200	Weak transcription	Adipose Nuclei	Adipose
45	chr5:43145400-43161400	Weak transcription	Duodenum Smooth Muscle	Duodenum
46	chr5:43145600-43156000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr5:43146400-43161200	Weak transcription	Liver	Liver
48	chr5:43146600-43161400	Weak transcription	HMEC	breast
49	chr5:43146600-43162200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr5:43147200-43155800	Weak transcription	Fetal Brain Female	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links