Variant report

Variant	rs73883415
Chromosome Location	chr3:179667851-179667852
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs59195034	1.00[AFR][1000 genomes]
rs59672007	1.00[AFR][1000 genomes]
rs60635140	0.81[AFR][1000 genomes]
rs73883412	1.00[AFR][1000 genomes]
rs73883413	1.00[AFR][1000 genomes]
rs73883414	1.00[AFR][1000 genomes]
rs73883420	1.00[AFR][1000 genomes]
rs73883423	1.00[AFR][1000 genomes]
rs73883425	1.00[AFR][1000 genomes]
rs73883427	1.00[AFR][1000 genomes]
rs73883429	1.00[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	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv534210	chr3:179666123-179899347	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 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	chr3:179660600-179680800	Weak transcription	Pancreas	Pancrea
2	chr3:179661200-179671400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr3:179666000-179670200	Enhancers	Brain Cingulate Gyrus	brain
4	chr3:179666200-179669000	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr3:179666200-179669000	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr3:179666200-179669400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:179666400-179668800	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:179666400-179670200	Enhancers	Brain Hippocampus Middle	brain
9	chr3:179666800-179669000	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr3:179667000-179668800	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr3:179667200-179668000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:179667200-179668800	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr3:179667200-179669000	Enhancers	Brain Substantia Nigra	brain
14	chr3:179667400-179668000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
15	chr3:179667400-179668000	Enhancers	Ovary	ovary
16	chr3:179667400-179668000	Enhancers	Thymus	Thymus
17	chr3:179667400-179668000	Enhancers	GM12878-XiMat	blood
18	chr3:179667400-179668800	Enhancers	H9 Cell Line	embryonic stem cell
19	chr3:179667400-179668800	Enhancers	Fetal Kidney	kidney
20	chr3:179667400-179668800	Enhancers	Fetal Thymus	thymus
21	chr3:179667400-179669000	Enhancers	Brain Angular Gyrus	brain
22	chr3:179667600-179668000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr3:179667600-179668000	Bivalent Enhancer	Brain Anterior Caudate	brain
24	chr3:179667600-179668600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr3:179667600-179668800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr3:179667600-179668800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:179667800-179669000	Genic enhancers	Dnd41	blood

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