Variant report

Variant	rs491970
Chromosome Location	chr3:43133056-43133057
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10865926	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4683359	0.92[AFR][1000 genomes]
rs535994	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs552472	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs614993	1.00[YRI][hapmap]
rs632013	1.00[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs664197	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs674118	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs939436	0.95[AFR][1000 genomes]
rs9828191	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460522	chr3:42967597-43175207	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv590149	chr3:42967597-43175207	Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv834672	chr3:43132722-43306272	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43119600-43135000	Weak transcription	Psoas Muscle	Psoas
2	chr3:43119800-43143800	Weak transcription	Fetal Heart	heart
3	chr3:43122400-43134400	Weak transcription	HepG2	liver
4	chr3:43122400-43145800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr3:43122600-43145200	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr3:43122800-43134800	Weak transcription	Brain Substantia Nigra	brain
7	chr3:43122800-43136000	Weak transcription	Pancreas	Pancrea
8	chr3:43122800-43136400	Weak transcription	HSMMtube	muscle
9	chr3:43122800-43145600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr3:43123000-43135200	Weak transcription	Brain Angular Gyrus	brain
11	chr3:43123000-43136000	Weak transcription	Right Ventricle	heart
12	chr3:43123000-43144400	Weak transcription	Fetal Intestine Large	intestine
13	chr3:43123000-43146400	Weak transcription	Duodenum Mucosa	Duodenum
14	chr3:43123000-43146600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr3:43123200-43140400	Weak transcription	Gastric	stomach
16	chr3:43123200-43144400	Weak transcription	Spleen	Spleen
17	chr3:43123200-43145000	Weak transcription	Adipose Nuclei	Adipose
18	chr3:43123400-43146400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr3:43123600-43135000	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr3:43123600-43135400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr3:43123600-43143600	Weak transcription	Lung	lung
22	chr3:43123600-43146600	Weak transcription	Fetal Intestine Small	intestine
23	chr3:43123800-43136400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr3:43124000-43133400	Weak transcription	Fetal Brain Male	brain
25	chr3:43124000-43134600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr3:43124200-43135600	Weak transcription	Fetal Brain Female	brain
27	chr3:43124200-43145000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr3:43124400-43135600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr3:43124400-43136200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:43124400-43136200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr3:43124400-43144200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
32	chr3:43124400-43146000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr3:43124400-43146600	Weak transcription	Aorta	Aorta
34	chr3:43124600-43138600	Weak transcription	Thymus	Thymus
35	chr3:43124600-43144800	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr3:43124600-43146800	Weak transcription	Primary hematopoietic stem cells	blood
37	chr3:43127000-43144400	Weak transcription	Dnd41	blood
38	chr3:43128400-43134600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr3:43128600-43134600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr3:43129000-43139600	Weak transcription	Liver	Liver
41	chr3:43129200-43136000	Weak transcription	Esophagus	oesophagus
42	chr3:43129200-43144000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr3:43130200-43134600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
44	chr3:43130400-43133800	Weak transcription	Left Ventricle	heart
45	chr3:43130600-43133400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr3:43130600-43134400	Weak transcription	Brain Hippocampus Middle	brain
47	chr3:43131200-43134600	Weak transcription	Fetal Muscle Trunk	muscle
48	chr3:43131600-43136600	Weak transcription	Fetal Stomach	stomach
49	chr3:43131600-43145600	Weak transcription	Primary T cells from cord blood	blood
50	chr3:43132000-43133600	Enhancers	Colon Smooth Muscle	Colon

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