Variant report

Variant	rs16853508
Chromosome Location	chr3:143096367-143096368
allele	C/T
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:17)

rs_ID	r²[population]
rs10513199	1.00[AMR][1000 genomes]
rs11925776	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16853511	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16853527	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16853529	1.00[AMR][1000 genomes]
rs34043464	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57334336	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57687610	1.00[AMR][1000 genomes]
rs58810476	1.00[AMR][1000 genomes]
rs72992119	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72992127	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72992135	0.84[AFR][1000 genomes]
rs72992177	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs72992193	1.00[AMR][1000 genomes]
rs72992195	1.00[AMR][1000 genomes]
rs72992201	1.00[AMR][1000 genomes]
rs7610768	1.00[AMR][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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	esv2757894	chr3:142992697-143285979	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	esv2759184	chr3:142992697-143285979	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
4	nsv877564	chr3:143059952-143116883	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv877565	chr3:143078986-143116883	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv999000	chr3:143086325-143136128	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143071600-143102400	Weak transcription	Esophagus	oesophagus
2	chr3:143072000-143099400	Weak transcription	Ovary	ovary
3	chr3:143077400-143104800	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:143082400-143102200	Weak transcription	Primary B cells from cord blood	blood
5	chr3:143083000-143096600	Weak transcription	Primary T cells from cord blood	blood
6	chr3:143083400-143098000	Weak transcription	Monocytes-CD14+_RO01746	blood
7	chr3:143085800-143103200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr3:143088400-143096800	Weak transcription	Dnd41	blood
9	chr3:143088800-143099800	Weak transcription	Aorta	Aorta
10	chr3:143094000-143099400	Weak transcription	Spleen	Spleen
11	chr3:143094000-143099600	Weak transcription	Adipose Nuclei	Adipose
12	chr3:143095000-143096600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr3:143096000-143098200	Enhancers	iPS-18 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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