Variant report

Variant	rs11133831
Chromosome Location	chr5:1629182-1629183
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 66 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10512659	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11948870	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11951409	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11951807	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11951980	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11952238	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11953233	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11954077	1.00[ASN][1000 genomes]
rs11955967	1.00[ASN][1000 genomes]
rs11957991	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11958097	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13165826	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2883372	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4415117	1.00[ASN][1000 genomes]
rs55864560	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55867519	0.97[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55957581	0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56185279	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58452381	1.00[ASN][1000 genomes]
rs58687576	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59610035	1.00[ASN][1000 genomes]
rs59656356	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59806631	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61340395	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6867199	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6869310	1.00[ASN][1000 genomes]
rs6870117	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6871261	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6872202	1.00[ASN][1000 genomes]
rs6884318	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6888170	1.00[ASN][1000 genomes]
rs6888910	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6889629	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6889684	0.83[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6891099	1.00[ASN][1000 genomes]
rs6898538	1.00[ASN][1000 genomes]
rs72717589	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72717593	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72717595	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72717596	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72717598	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72717600	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73732121	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73732122	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73732123	0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs73732124	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73732134	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7708447	1.00[ASN][1000 genomes]
rs7716004	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7725592	1.00[ASN][1000 genomes]
rs7728463	1.00[ASN][1000 genomes]
rs7728632	1.00[ASN][1000 genomes]
rs7729323	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7732756	1.00[ASN][1000 genomes]
rs7736524	0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7736669	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7737033	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7737331	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[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	nsv933805	chr5:1450724-1941619	Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv880740	chr5:1468287-1671200	Weak transcription Strong transcription Active TSS Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
3	nsv881554	chr5:1468287-1696932	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	49 gene(s)	inside rSNPs	diseases
4	nsv817407	chr5:1495354-2191460	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	107 gene(s)	inside rSNPs	diseases
5	nsv881096	chr5:1503610-1671200	Flanking Bivalent TSS/Enh Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
6	nsv10657	chr5:1544428-1633373	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
7	nsv964815	chr5:1608931-1639317	Strong transcription Active TSS Weak transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv880390	chr5:1612612-1653418	Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs11133831	SDHAP3	cis	Thyroid	GTEx
rs11133831	SDHAP3	cis	Whole Blood	GTEx
rs11133831	LOC728613///PDCD6	Cis_1M	lymphoblastoid	RTeQTL
rs11133831	CTD-2012J19.3	cis	Esophagus Mucosa	GTEx
rs11133831	SDHAP3	cis	Esophagus Mucosa	GTEx
rs11133831	SDHAP3	cis	Nerve Tibial	GTEx
rs11133831	SDHAP3	cis	Artery Tibial	GTEx
rs11133831	RP11-43F13.1	cis	Whole Blood	GTEx
rs11133831	SDHAP3	cis	Esophagus Muscularis	GTEx

Chromatin state (count:97 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:1595000-1634000	Weak transcription	Stomach Mucosa	stomach
2	chr5:1595200-1632800	Weak transcription	Brain Angular Gyrus	brain
3	chr5:1595200-1632800	Weak transcription	Right Ventricle	heart
4	chr5:1595400-1633200	Weak transcription	Primary B cells from cord blood	blood
5	chr5:1595400-1633200	Weak transcription	Brain Cingulate Gyrus	brain
6	chr5:1595400-1633200	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr5:1595400-1633200	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr5:1597600-1632600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr5:1597600-1632800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr5:1597600-1632800	Weak transcription	Rectal Smooth Muscle	rectum
11	chr5:1597600-1633000	Weak transcription	Brain Hippocampus Middle	brain
12	chr5:1601400-1632800	Weak transcription	Hela-S3	cervix
13	chr5:1606200-1633200	Weak transcription	Brain Anterior Caudate	brain
14	chr5:1608800-1632800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr5:1608800-1633800	Weak transcription	Fetal Lung	lung
16	chr5:1609200-1633200	Weak transcription	Primary T helper cells PMA-I stimulated	--
17	chr5:1609200-1633200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr5:1609600-1633600	Weak transcription	Left Ventricle	heart
19	chr5:1610000-1633400	Weak transcription	Colonic Mucosa	Colon
20	chr5:1610600-1632800	Weak transcription	NHEK	skin
21	chr5:1610600-1633200	Weak transcription	Colon Smooth Muscle	Colon
22	chr5:1611800-1633800	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr5:1613200-1633200	Weak transcription	HSMMtube	muscle
24	chr5:1613800-1633800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr5:1617000-1633200	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr5:1617400-1632600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
27	chr5:1617400-1633200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr5:1619000-1633200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr5:1619400-1632800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr5:1619400-1633800	Weak transcription	Primary monocytes fromperipheralblood	blood
31	chr5:1619600-1632400	Weak transcription	Primary T cells fromperipheralblood	blood
32	chr5:1619600-1632800	Weak transcription	GM12878-XiMat	blood
33	chr5:1619600-1633000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr5:1619600-1633800	Weak transcription	Placenta	Placenta
35	chr5:1620000-1630400	Weak transcription	Fetal Brain Female	brain
36	chr5:1620000-1633800	Weak transcription	Lung	lung
37	chr5:1620200-1629400	Weak transcription	Gastric	stomach
38	chr5:1620400-1633800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr5:1621600-1633200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr5:1621600-1633200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr5:1621800-1632800	Weak transcription	Primary B cells from peripheral blood	blood
42	chr5:1622000-1633200	Weak transcription	Duodenum Mucosa	Duodenum
43	chr5:1622200-1633800	Weak transcription	Fetal Kidney	kidney
44	chr5:1622600-1632800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr5:1623200-1633200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr5:1623400-1633800	Weak transcription	Primary T cells from cord blood	blood
47	chr5:1624200-1633200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr5:1624400-1632800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr5:1624400-1633200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr5:1624400-1633200	Weak transcription	HUES48 Cell Line	embryonic stem cell

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