Variant report

Variant	rs13353903
Chromosome Location	chr5:79568216-79568217
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10037587	0.87[EUR][1000 genomes]
rs10054681	0.93[EUR][1000 genomes]
rs10056958	0.93[EUR][1000 genomes]
rs10071189	0.92[EUR][1000 genomes]
rs10474614	0.92[EUR][1000 genomes]
rs13360748	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13361029	0.93[EUR][1000 genomes]
rs28424275	0.93[EUR][1000 genomes]
rs6453511	0.86[ASN][1000 genomes]
rs72778013	0.93[EUR][1000 genomes]
rs72778033	0.93[EUR][1000 genomes]
rs9293808	0.82[EUR][1000 genomes]
rs9293811	0.93[EUR][1000 genomes]
rs9654436	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432748	chr5:79300434-79577760	Enhancers Genic enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv948807	chr5:79549207-79805765	Genic enhancers Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 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	chr5:79553400-79577800	Weak transcription	Right Atrium	heart
2	chr5:79561600-79569800	Enhancers	Primary T cells from cord blood	blood
3	chr5:79563600-79569200	Enhancers	Primary T cells fromperipheralblood	blood
4	chr5:79563800-79569400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
5	chr5:79563800-79569400	Enhancers	Fetal Thymus	thymus
6	chr5:79566400-79569400	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chr5:79567000-79571000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr5:79567800-79571000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr5:79567800-79580400	Weak transcription	Primary T helper cells fromperipheralblood	blood
10	chr5:79568000-79568400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
11	chr5:79568000-79569000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr5:79568200-79568400	Enhancers	iPS DF 19.11 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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