Variant report

Variant	rs152717
Chromosome Location	chr5:14621652-14621653
allele	A/C
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]
rs13172589	0.87[EUR][1000 genomes]
rs149196	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs149197	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs153819	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs153823	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs153824	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs171652	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2455395	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs25958	0.89[EUR][1000 genomes]
rs25959	0.87[EUR][1000 genomes]
rs26179	0.87[EUR][1000 genomes]
rs27354	0.89[EUR][1000 genomes]
rs31971	0.85[EUR][1000 genomes]
rs31972	0.82[EUR][1000 genomes]
rs31974	0.85[EUR][1000 genomes]
rs31976	0.87[EUR][1000 genomes]
rs36103605	0.85[EUR][1000 genomes]
rs457897	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs468184	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][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	nsv1026914	chr5:14237782-14751588	Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv1018187	chr5:14385164-15127103	Strong transcription Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
3	nsv830211	chr5:14474675-14675776	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1032951	chr5:14529579-14667342	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:14594400-14621800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr5:14602000-14621800	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr5:14608800-14623000	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr5:14609200-14622800	Strong transcription	Monocytes-CD14+_RO01746	blood
5	chr5:14610800-14624000	Weak transcription	Lung	lung
6	chr5:14612200-14623600	Weak transcription	Placenta	Placenta
7	chr5:14616800-14625400	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr5:14617800-14622200	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr5:14618000-14622000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr5:14619800-14626200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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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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