Variant report

Variant	rs716848
Chromosome Location	chr5:96265000-96265001
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 115 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:107)

rs_ID	r²[population]
rs10038651	0.86[EUR][1000 genomes]
rs10044354	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs10051637	0.88[CEU][hapmap];0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10058476	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10077945	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10434709	0.85[CEU][hapmap]
rs1046395	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1046396	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10476696	0.86[EUR][1000 genomes]
rs11135484	0.85[CEU][hapmap]
rs1216566	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1216567	0.99[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1216571	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12516666	0.85[CEU][hapmap]
rs13167902	0.85[CEU][hapmap]
rs13170029	0.92[EUR][1000 genomes]
rs13358339	0.86[EUR][1000 genomes]
rs1363907	0.96[CEU][hapmap];0.84[CHB][hapmap];0.88[JPT][hapmap];0.87[YRI][hapmap];0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1363908	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1363974	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs1363976	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1423357	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs1423566	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1477364	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1544777	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1559355	0.85[CEU][hapmap]
rs1820148	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1974871	0.88[CEU][hapmap];0.81[YRI][hapmap]
rs2113050	0.80[CEU][hapmap]
rs2161548	0.89[CEU][hapmap];0.86[EUR][1000 genomes]
rs2247650	0.82[CEU][hapmap]
rs2278018	0.85[CEU][hapmap]
rs2278019	0.85[CEU][hapmap]
rs2351010	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs2351011	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2432141	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2432142	0.84[EUR][1000 genomes]
rs251339	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs251340	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs251341	0.86[AFR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs251343	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2548224	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2548226	0.90[AFR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2548516	0.89[EUR][1000 genomes]
rs2548529	0.90[CHB][hapmap];0.81[JPT][hapmap]
rs2548530	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2548532	0.96[CEU][hapmap];0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2549783	1.00[CEU][hapmap];0.92[YRI][hapmap];0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs2549784	0.84[YRI][hapmap]
rs2549794	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2617435	0.81[EUR][1000 genomes]
rs2617439	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2617447	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs27289	0.84[EUR][1000 genomes]
rs27290	0.88[CEU][hapmap];0.84[EUR][1000 genomes]
rs27293	0.84[EUR][1000 genomes]
rs27295	0.84[EUR][1000 genomes]
rs27300	0.88[CEU][hapmap];0.80[EUR][1000 genomes]
rs27306	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[YRI][hapmap];0.89[EUR][1000 genomes]
rs27307	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.89[EUR][1000 genomes]
rs27436	0.85[CEU][hapmap];0.84[EUR][1000 genomes]
rs2762	0.80[CEU][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs27659	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs27660	0.89[EUR][1000 genomes]
rs27711	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[YRI][hapmap];0.89[EUR][1000 genomes]
rs27712	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[EUR][1000 genomes]
rs27993	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.88[YRI][hapmap];0.89[EUR][1000 genomes]
rs2859491	0.96[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2910686	0.86[CEU][hapmap];0.90[EUR][1000 genomes]
rs2910687	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2910788	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2910789	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2910793	0.94[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2927608	0.89[EUR][1000 genomes]
rs2927609	1.00[CEU][hapmap];0.89[CHB][hapmap];0.94[JPT][hapmap];0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3734015	0.85[CEU][hapmap]
rs3797796	0.96[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.92[YRI][hapmap];0.84[EUR][1000 genomes]
rs38029	0.89[EUR][1000 genomes]
rs38031	0.89[EUR][1000 genomes]
rs38032	0.96[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.86[YRI][hapmap];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs38033	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs38034	0.85[CEU][hapmap];0.87[EUR][1000 genomes]
rs38038	0.84[EUR][1000 genomes]
rs38039	0.89[EUR][1000 genomes]
rs38042	0.82[CEU][hapmap]
rs38043	0.89[CEU][hapmap];0.84[EUR][1000 genomes]
rs38044	0.84[EUR][1000 genomes]
rs3849749	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.92[YRI][hapmap];0.90[AFR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3909451	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs39602	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs4360063	0.89[CEU][hapmap];0.87[EUR][1000 genomes]
rs4869313	0.80[EUR][1000 genomes]
rs4869314	0.85[CEU][hapmap]
rs55770741	0.83[EUR][1000 genomes]
rs6556942	0.96[CEU][hapmap];0.80[JPT][hapmap];0.89[YRI][hapmap];0.83[EUR][1000 genomes]
rs6859168	0.82[AFR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6871162	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6873866	0.84[AFR][1000 genomes]
rs6887500	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7703341	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7716222	0.88[CEU][hapmap];0.86[EUR][1000 genomes]
rs7719705	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7726445	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7731592	0.89[CEU][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7733312	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9127	0.92[CEU][hapmap]
rs9314181	0.86[EUR][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	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv948703	chr5:96078309-96368839	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1027472	chr5:96081592-96337550	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1028741	chr5:96082401-96372165	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv949058	chr5:96082433-96390619	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv598963	chr5:96084776-96363407	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv531967	chr5:96127842-96302702	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs716848	ERAP2	cis	Esophagus Mucosa	GTEx
rs716848	ERAP2	cis	Whole Blood	GTEx
rs716848	ERAP2	cis	Artery Tibial	GTEx
rs716848	LNPEP	cis	Esophagus Muscularis	GTEx
rs716848	ERAP2	cis	Muscle Skeletal	GTEx
rs716848	AC008865.1	cis	Artery Tibial	GTEx
rs716848	ERAP2	cis	Skin Sun Exposed Lower leg	GTEx
rs716848	LRAP	cis	normal skin	skin_eQTL
rs716848	LRAP	Cis_1M	lymphoblastoid	RTeQTL
rs716848	ERAP2	cis	Thyroid	GTEx
rs716848	LRAP	cis	uninvolved skin	skin_eQTL
rs716848	ERAP2	cis	Adipose Subcutaneous	GTEx
rs716848	ERAP2	cis	Esophagus Muscularis	GTEx
rs716848	ERAP2	cis	lung	GTEx
rs716848	ERAP2	cis	Stomach	GTEx
rs716848	ERAP2	cis	Artery Aorta	GTEx
rs716848	LRAP	cis	lesional skin	skin_eQTL
rs716848	ERAP2	cis	Heart Left Ventricle	GTEx
rs716848	ERAP2	cis	Nerve Tibial	GTEx

Chromatin state (count:72 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96221600-96269200	Weak transcription	Fetal Brain Male	brain
2	chr5:96222000-96268600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr5:96225600-96266400	Weak transcription	Gastric	stomach
4	chr5:96229600-96269600	Weak transcription	Aorta	Aorta
5	chr5:96229800-96270000	Weak transcription	Esophagus	oesophagus
6	chr5:96237400-96269200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr5:96237800-96265000	Weak transcription	Fetal Muscle Leg	muscle
8	chr5:96239800-96268000	Weak transcription	Colonic Mucosa	Colon
9	chr5:96242200-96268000	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr5:96243600-96266400	Weak transcription	Brain Angular Gyrus	brain
11	chr5:96246000-96268200	Weak transcription	Fetal Intestine Small	intestine
12	chr5:96246000-96270200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:96249600-96267800	Weak transcription	Fetal Intestine Large	intestine
14	chr5:96249800-96270000	Weak transcription	Lung	lung
15	chr5:96253800-96265800	Weak transcription	Thymus	Thymus
16	chr5:96254000-96267200	Weak transcription	Adipose Nuclei	Adipose
17	chr5:96254000-96268600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
18	chr5:96256000-96266400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr5:96256200-96267000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr5:96256400-96266600	Weak transcription	Primary B cells from cord blood	blood
21	chr5:96257200-96265800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr5:96257400-96269600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr5:96257800-96267400	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr5:96258800-96267600	Weak transcription	Brain Substantia Nigra	brain
25	chr5:96259800-96267400	Weak transcription	Brain Anterior Caudate	brain
26	chr5:96260000-96265800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr5:96260000-96266400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr5:96260200-96267800	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr5:96260200-96268200	Weak transcription	HMEC	breast
30	chr5:96260200-96269000	Weak transcription	Fetal Stomach	stomach
31	chr5:96260200-96269400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr5:96260400-96267400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr5:96260400-96267400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr5:96260400-96268200	Weak transcription	NHEK	skin
35	chr5:96260600-96268600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr5:96261600-96267000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr5:96263000-96267000	Weak transcription	Primary monocytes fromperipheralblood	blood
38	chr5:96263000-96267000	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr5:96263800-96265600	Enhancers	K562	blood
40	chr5:96264000-96265400	Enhancers	Primary T helper naive cells from peripheral blood	blood
41	chr5:96264000-96266800	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr5:96264000-96268000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr5:96264000-96268200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr5:96264000-96269200	Enhancers	Fetal Heart	heart
45	chr5:96264200-96265000	Enhancers	Primary B cells from peripheral blood	blood
46	chr5:96264200-96266400	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr5:96264200-96268000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr5:96264200-96268000	Enhancers	Primary T killer memory cells from peripheral blood	blood
49	chr5:96264400-96267600	Enhancers	Primary T helper cells PMA-I stimulated	--
50	chr5:96264400-96267800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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