Variant report

Variant	rs298521
Chromosome Location	chr5:17312669-17312670
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs298514	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs298519	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][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	nsv880277	chr5:16829442-17316288	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv1029959	chr5:17133214-17455995	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
3	nsv461988	chr5:17296342-17484038	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv597313	chr5:17296342-17484038	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	esv3356359	chr5:17310802-17313300	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:17306200-17315200	Weak transcription	NHLF	lung
2	chr5:17306800-17315000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:17307000-17314800	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr5:17307000-17315400	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr5:17307000-17316000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:17307000-17317000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr5:17307000-17320200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr5:17307400-17316000	Weak transcription	Placenta	Placenta
9	chr5:17309800-17314800	Weak transcription	Hela-S3	cervix
10	chr5:17310400-17316000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr5:17311000-17316200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr5:17311400-17314800	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr5:17312200-17312800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr5:17312400-17313200	Flanking Active TSS	A549	lung
15	chr5:17312400-17313800	Enhancers	Stomach Mucosa	stomach
16	chr5:17312600-17312800	Enhancers	Rectal Mucosa Donor 31	rectum
17	chr5:17312600-17313000	Enhancers	Fetal Lung	lung
18	chr5:17312600-17314600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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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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