Variant report

Variant	rs56220520
Chromosome Location	chr16:82901698-82901699
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:6)

rs_ID	r²[population]
rs58804740	1.00[AFR][1000 genomes]
rs61538662	0.95[AFR][1000 genomes]
rs74029073	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74029260	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74029263	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74032603	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
2	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv1057341	chr16:82363800-83198907	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
4	nsv542997	chr16:82363800-83198907	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
5	nsv1063617	chr16:82786803-83229529	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	esv2830385	chr16:82841335-82950413	Enhancers ZNF genes & repeats Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82879200-82907000	Weak transcription	Left Ventricle	heart
2	chr16:82886200-82917000	Weak transcription	Right Ventricle	heart
3	chr16:82891000-82907000	Weak transcription	Psoas Muscle	Psoas
4	chr16:82891600-82907800	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr16:82897800-82905200	Weak transcription	HSMM	muscle
6	chr16:82898400-82904600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr16:82899400-82904800	Weak transcription	HSMMtube	muscle
8	chr16:82899400-82909800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr16:82899800-82904600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr16:82900200-82902600	Enhancers	Fetal Intestine Large	intestine
11	chr16:82901000-82902800	Enhancers	Duodenum Mucosa	Duodenum
12	chr16:82901200-82904800	Weak transcription	Aorta	Aorta
13	chr16:82901200-82910400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr16:82901600-82902000	Weak transcription	Fetal Intestine Small	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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