Variant report

Variant	rs2310986
Chromosome Location	chr17:20705402-20705403
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11656284	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12938949	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12941415	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12943312	0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2958458	0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2958474	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2958477	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2958478	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2993350	0.80[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34142266	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3930821	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3930822	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4985927	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6587086	0.82[EUR][1000 genomes]
rs7218490	0.94[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs8065742	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs8076473	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916440	chr17:20171468-20839266	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
2	esv2751619	chr17:20462908-20914156	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	esv3361931	chr17:20539962-20845258	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv469647	chr17:20552253-20751738	Flanking Active TSS Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv482489	chr17:20552253-20751738	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	esv3330516	chr17:20572433-20862663	Enhancers Bivalent/Poised TSS Genic enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	nsv907884	chr17:20613642-20715726	Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv9512	chr17:20703055-20709128	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv1811047	chr17:20703343-20708705	Bivalent Enhancer Active TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	esv32971	chr17:20703572-20705693	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20704600-20705600	Active TSS	A549	lung
2	chr17:20704800-20705600	Active TSS	HUES48 Cell Line	embryonic stem cell
3	chr17:20704800-20705600	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr17:20704800-20705600	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr17:20704800-20705600	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr17:20704800-20705600	Active TSS	iPS-20b Cell Line	embryonic stem cell
7	chr17:20704800-20705600	Active TSS	K562	blood
8	chr17:20705400-20706600	Weak transcription	Primary B cells from peripheral blood	blood
9	chr17:20705400-20706600	Weak transcription	Placenta	Placenta
10	chr17:20705400-20706800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr17:20705400-20707000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr17:20705400-20718000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

Quick Search:

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

what's new

Quick links