Variant report

Variant	rs34564407
Chromosome Location	chr5:79813356-79813357
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:11)

rs_ID	r²[population]
rs13160975	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs13166575	0.83[AFR][1000 genomes]
rs34093562	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34691034	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34792001	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35587631	0.95[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs36153861	0.81[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs62365285	0.84[AFR][1000 genomes]
rs71636230	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs71636231	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs71636234	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028027	chr5:79694699-79841752	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers 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

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:79784800-79819400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr5:79785000-79822800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr5:79785200-79817600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr5:79799000-79817400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:79800000-79817000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr5:79800000-79825600	Weak transcription	Primary hematopoietic stem cells	blood
7	chr5:79800600-79825200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr5:79801400-79825400	Weak transcription	Pancreas	Pancrea
9	chr5:79801600-79818000	Weak transcription	Ovary	ovary
10	chr5:79802200-79820800	Weak transcription	Brain Cingulate Gyrus	brain
11	chr5:79802600-79820000	Weak transcription	Fetal Stomach	stomach
12	chr5:79805200-79824200	Strong transcription	Monocytes-CD14+_RO01746	blood
13	chr5:79805400-79816200	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr5:79806000-79816000	Weak transcription	Brain Angular Gyrus	brain
15	chr5:79806200-79815800	Weak transcription	Brain Anterior Caudate	brain
16	chr5:79806200-79825600	Weak transcription	HSMMtube	muscle
17	chr5:79807400-79817200	Weak transcription	Aorta	Aorta
18	chr5:79807400-79825600	Weak transcription	Osteobl	bone
19	chr5:79807600-79819000	Weak transcription	NHDF-Ad	bronchial
20	chr5:79808600-79824400	Weak transcription	Fetal Lung	lung
21	chr5:79810400-79825600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr5:79811200-79816400	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr5:79812400-79813400	Enhancers	Hela-S3	cervix
24	chr5:79812800-79813400	Strong transcription	Adipose Nuclei	Adipose
25	chr5:79813000-79821800	Weak transcription	Esophagus	oesophagus
26	chr5:79813200-79815600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr5:79813200-79818000	Weak transcription	Placenta	Placenta
28	chr5:79813200-79820400	Weak transcription	HSMM	muscle
29	chr5:79813200-79824000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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