Variant report

Variant	rs16867541
Chromosome Location	chr5:88616004-88616005
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10514305	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1158150	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12653011	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12653245	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12659528	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16867551	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16867552	0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16867553	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16867554	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16867563	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2059853	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34814331	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56756608	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59842575	0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61418152	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6870380	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6876988	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6883052	0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6883088	0.90[EUR][1000 genomes];0.87[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	nsv532159	chr5:88016214-88783092	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv533373	chr5:88062497-89028098	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
3	nsv529543	chr5:88348147-88783092	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv830387	chr5:88547862-88682442	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv830388	chr5:88578939-88793870	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:88612000-88618400	Weak transcription	Primary B cells from peripheral blood	blood
2	chr5:88612000-88619200	Weak transcription	Primary B cells from cord blood	blood
3	chr5:88615800-88616800	ZNF genes & repeats	GM12878-XiMat	blood

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