Variant report

Variant	rs8048023
Chromosome Location	chr16:47903315-47903316
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs13336450	0.93[AFR][1000 genomes]
rs1985323	0.86[YRI][hapmap]
rs28415596	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28421488	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6500353	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs6500354	0.86[AFR][1000 genomes]
rs7202593	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7205450	0.83[AFR][1000 genomes]
rs8045787	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8045788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8045934	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs8048189	0.83[AFR][1000 genomes]
rs8054600	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9921499	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9926879	1.00[YRI][hapmap]
rs9929891	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9931056	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9935449	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs9939344	0.94[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	nsv520355	chr16:47424828-48164777	Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv525976	chr16:47583872-48035026	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv428657	chr16:47748036-47913816	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv833218	chr16:47869819-48051745	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:47900000-47905200	Weak transcription	Pancreas	Pancrea
2	chr16:47900200-47903600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr16:47900800-47904600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr16:47901000-47903800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr16:47901000-47903800	Weak transcription	Spleen	Spleen
6	chr16:47901000-47905800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr16:47901000-47911000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr16:47901200-47905200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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Input of quick search could be:

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

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