Variant report

Variant	rs58960032
Chromosome Location	chr16:82073686-82073687
allele	A/C
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]
rs16956276	0.98[AFR][1000 genomes]
rs16956279	0.98[AFR][1000 genomes]
rs16956282	0.95[AFR][1000 genomes]
rs16956292	0.90[AFR][1000 genomes]
rs16956326	0.83[AMR][1000 genomes]
rs4258604	0.83[AMR][1000 genomes]
rs7203108	0.83[AMR][1000 genomes]
rs73600767	0.92[AFR][1000 genomes]
rs73600769	0.87[AFR][1000 genomes]
rs8191071	0.82[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	nsv907012	chr16:81986896-82115148	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1058368	chr16:82029516-82152788	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv532598	chr16:82034475-82738733	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82067400-82077000	Weak transcription	Right Atrium	heart
2	chr16:82068800-82077400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr16:82069200-82074000	Weak transcription	Fetal Lung	lung
4	chr16:82069200-82076600	Weak transcription	HSMMtube	muscle
5	chr16:82069200-82077400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr16:82069400-82075200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr16:82070200-82083400	Weak transcription	Colonic Mucosa	Colon
8	chr16:82070800-82074200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr16:82070800-82074800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr16:82070800-82081200	Weak transcription	Pancreas	Pancrea
11	chr16:82071800-82077800	Weak transcription	Stomach Mucosa	stomach
12	chr16:82072800-82074800	Weak transcription	Fetal Intestine Small	intestine
13	chr16:82072800-82075000	Weak transcription	Fetal Intestine Large	intestine
14	chr16:82072800-82077800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr16:82072800-82077800	Enhancers	Liver	Liver
16	chr16:82072800-82077800	Weak transcription	Gastric	stomach
17	chr16:82072800-82077800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr16:82073000-82073800	Genic enhancers	Duodenum Mucosa	Duodenum
19	chr16:82073000-82076600	Weak transcription	Fetal Kidney	kidney
20	chr16:82073200-82074200	Weak transcription	HepG2	liver
21	chr16:82073400-82074800	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr16:82073600-82075200	Weak transcription	Placenta	Placenta

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