Variant report

Variant	rs834166
Chromosome Location	chr3:43076674-43076675
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs13061038	0.80[EUR][1000 genomes]
rs2936817	0.81[EUR][1000 genomes]
rs643663	0.81[EUR][1000 genomes]
rs658958	0.80[EUR][1000 genomes]
rs697327	0.82[EUR][1000 genomes]
rs834191	0.83[ASN][1000 genomes]
rs870238	0.81[EUR][1000 genomes]
rs9311333	0.81[EUR][1000 genomes]
rs9882262	0.81[EUR][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	nsv432417	chr3:43045796-43098296	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43059600-43084600	Weak transcription	Pancreas	Pancrea
2	chr3:43061000-43080200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr3:43063000-43077400	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:43063600-43084800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr3:43064000-43077800	Weak transcription	Brain Substantia Nigra	brain
6	chr3:43065400-43084400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr3:43067600-43084000	Weak transcription	Aorta	Aorta
8	chr3:43068200-43076800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr3:43070600-43084800	Weak transcription	Esophagus	oesophagus
10	chr3:43073400-43077200	Weak transcription	Stomach Mucosa	stomach
11	chr3:43073400-43077600	Weak transcription	Brain Cingulate Gyrus	brain
12	chr3:43073400-43077800	Weak transcription	Fetal Intestine Large	intestine
13	chr3:43073400-43084600	Weak transcription	Brain Angular Gyrus	brain
14	chr3:43073400-43084600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr3:43073600-43084400	Weak transcription	Adipose Nuclei	Adipose
16	chr3:43074000-43078400	Strong transcription	Placenta	Placenta
17	chr3:43074600-43084200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr3:43074800-43081200	Weak transcription	Fetal Intestine Small	intestine
19	chr3:43075200-43084200	Weak transcription	Ovary	ovary
20	chr3:43075400-43078200	Weak transcription	Liver	Liver
21	chr3:43075800-43076800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:43076200-43078800	Strong transcription	Fetal Stomach	stomach
23	chr3:43076200-43079000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr3:43076400-43077200	ZNF genes & repeats	Stomach Smooth Muscle	stomach
25	chr3:43076400-43077600	Enhancers	Fetal Muscle Trunk	muscle
26	chr3:43076600-43078800	Enhancers	Primary T cells fromperipheralblood	blood
27	chr3:43076600-43079000	Enhancers	Fetal Muscle Leg	muscle

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