Variant report

Variant	rs10499182
Chromosome Location	chr6:131493409-131493410
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs11965549	0.93[GIH][hapmap];0.88[TSI][hapmap];0.87[EUR][1000 genomes]
rs17060065	0.88[CEU][hapmap];0.87[EUR][1000 genomes]
rs17787339	0.88[CEU][hapmap];0.93[GIH][hapmap];0.88[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17787538	0.82[CEU][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55752298	0.87[EUR][1000 genomes]
rs60118432	0.93[EUR][1000 genomes]
rs73633185	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032955	chr6:131298803-131818502	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
2	nsv538443	chr6:131298803-131818502	Active TSS Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
3	nsv830807	chr6:131390952-131581931	Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv886664	chr6:131443843-131754930	Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10499182	TAAR1	cis	cerebellum	SCAN

Chromatin state (count:77 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:131457200-131504400	Weak transcription	Spleen	Spleen
2	chr6:131457600-131505600	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr6:131457600-131520800	Weak transcription	Right Ventricle	heart
4	chr6:131457800-131504200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr6:131457800-131504200	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr6:131458000-131498800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:131458000-131505600	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr6:131458000-131505800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:131458200-131505200	Weak transcription	Fetal Lung	lung
10	chr6:131458200-131513400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:131458400-131498000	Weak transcription	Aorta	Aorta
12	chr6:131458400-131504200	Weak transcription	Dnd41	blood
13	chr6:131461200-131494600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr6:131464000-131499200	Weak transcription	Fetal Stomach	stomach
15	chr6:131464800-131499200	Weak transcription	Esophagus	oesophagus
16	chr6:131468200-131499800	Weak transcription	Lung	lung
17	chr6:131469200-131504200	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr6:131481200-131494600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr6:131481200-131504400	Weak transcription	HSMM	muscle
20	chr6:131483000-131506200	Weak transcription	Primary monocytes fromperipheralblood	blood
21	chr6:131483600-131504200	Weak transcription	Pancreas	Pancrea
22	chr6:131484000-131504200	Weak transcription	Primary T cells from cord blood	blood
23	chr6:131484200-131504400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr6:131484400-131509200	Weak transcription	Rectal Smooth Muscle	rectum
25	chr6:131485000-131504200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr6:131485200-131504200	Weak transcription	Primary B cells from peripheral blood	blood
27	chr6:131485400-131504400	Weak transcription	H9 Cell Line	embryonic stem cell
28	chr6:131485400-131509600	Weak transcription	Small Intestine	intestine
29	chr6:131485600-131494600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:131485600-131504200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr6:131485600-131514000	Weak transcription	Rectal Mucosa Donor 29	rectum
32	chr6:131485800-131504200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr6:131486000-131494400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr6:131486000-131498400	Weak transcription	Fetal Intestine Large	intestine
35	chr6:131486000-131504200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr6:131486000-131505000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr6:131486000-131505600	Weak transcription	HepG2	liver
38	chr6:131486200-131494400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr6:131486200-131494600	Weak transcription	Brain Anterior Caudate	brain
40	chr6:131486200-131494600	Weak transcription	Brain Substantia Nigra	brain
41	chr6:131486200-131499000	Weak transcription	Brain Angular Gyrus	brain
42	chr6:131486200-131504200	Weak transcription	Brain Cingulate Gyrus	brain
43	chr6:131486200-131504200	Weak transcription	Brain Inferior Temporal Lobe	brain
44	chr6:131486200-131505800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:131486400-131493600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:131486400-131504600	Weak transcription	Fetal Intestine Small	intestine
47	chr6:131486400-131505000	Weak transcription	Placenta	Placenta
48	chr6:131487000-131504200	Weak transcription	Fetal Muscle Trunk	muscle
49	chr6:131487000-131505200	Weak transcription	Skeletal Muscle Female	skeletal muscle
50	chr6:131487000-131512800	Weak transcription	Brain Hippocampus Middle	brain

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