Variant report

Variant	rs16883546
Chromosome Location	chr8:113407427-113407428
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10505177	0.94[AFR][1000 genomes]
rs11991999	0.82[AFR][1000 genomes]
rs11992226	1.00[AFR][1000 genomes]
rs16883536	1.00[AFR][1000 genomes]
rs16883550	1.00[AFR][1000 genomes]
rs16883554	0.91[AFR][1000 genomes]
rs55756436	0.89[AFR][1000 genomes]
rs60746545	1.00[AFR][1000 genomes]
rs6999740	0.88[AFR][1000 genomes]
rs7000134	0.88[AFR][1000 genomes]
rs73700688	0.94[AFR][1000 genomes]
rs73700689	1.00[AFR][1000 genomes]
rs73700692	1.00[AFR][1000 genomes]
rs73700693	1.00[AFR][1000 genomes]
rs73700695	0.97[AFR][1000 genomes]
rs73700696	1.00[AFR][1000 genomes]
rs73704003	0.88[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533857	chr8:112819659-113801258	Enhancers Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
2	nsv1022457	chr8:113071774-113811177	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
3	esv2755868	chr8:113282795-113634842	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2753595	chr8:113283214-114190390	Enhancers Weak transcription Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	esv2754232	chr8:113294967-113634842	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:113399400-113410600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:113406400-113408000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
3	chr8:113406600-113408200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
4	chr8:113407200-113407600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
5	chr8:113407200-113409200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
6	chr8:113407200-113409400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr8:113407400-113407600	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
8	chr8:113407400-113408400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
9	chr8:113407400-113408800	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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