Variant report

Variant	rs73571857
Chromosome Location	chr16:71417122-71417123
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs28407180	1.00[AMR][1000 genomes]
rs28591533	1.00[AMR][1000 genomes]
rs55882565	0.83[AMR][1000 genomes]
rs7192486	1.00[AMR][1000 genomes]
rs7200566	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs7206080	0.83[AMR][1000 genomes]
rs7206706	1.00[AMR][1000 genomes]
rs74025979	0.86[AFR][1000 genomes]
rs8053156	0.83[AMR][1000 genomes]
rs8054267	1.00[AMR][1000 genomes]
rs8055003	1.00[AMR][1000 genomes]
rs8056365	1.00[AMR][1000 genomes]
rs8063972	1.00[AMR][1000 genomes]
rs9925993	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949461	chr16:71196153-71579711	ZNF genes & repeats Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
2	nsv1062426	chr16:71307180-71423400	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv572949	chr16:71352071-71426563	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	esv3417792	chr16:71416447-71419521	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:71398800-71419800	Weak transcription	Brain Germinal Matrix	brain
2	chr16:71414600-71418400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:71416400-71419400	Strong transcription	Adipose Nuclei	Adipose
4	chr16:71416600-71417400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr16:71416600-71417600	Enhancers	Placenta Amnion	Placenta Amnion
6	chr16:71416600-71417800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr16:71416600-71418400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr16:71416600-71419400	Enhancers	Esophagus	oesophagus
9	chr16:71416800-71417800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr16:71416800-71418000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr16:71416800-71420600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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