Variant report

Variant	rs13277523
Chromosome Location	chr8:99323831-99323832
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10282835	1.00[ASN][1000 genomes]
rs11785588	1.00[ASN][1000 genomes]
rs12386830	1.00[ASN][1000 genomes]
rs13282021	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs16896995	1.00[ASN][1000 genomes]
rs16897028	1.00[ASN][1000 genomes]
rs16897050	1.00[ASN][1000 genomes]
rs16897058	1.00[ASN][1000 genomes]
rs16897069	1.00[ASN][1000 genomes]
rs2443572	1.00[CEU][hapmap]
rs28621642	1.00[ASN][1000 genomes]
rs34018826	1.00[ASN][1000 genomes]
rs4615538	1.00[ASN][1000 genomes]
rs55793219	1.00[ASN][1000 genomes]
rs55921088	1.00[ASN][1000 genomes]
rs56214625	1.00[ASN][1000 genomes]
rs6982282	1.00[ASN][1000 genomes]
rs6982285	1.00[ASN][1000 genomes]
rs72666612	1.00[ASN][1000 genomes]
rs72666616	1.00[ASN][1000 genomes]
rs72666618	1.00[ASN][1000 genomes]
rs72666619	1.00[ASN][1000 genomes]
rs72666623	1.00[ASN][1000 genomes]
rs72666624	1.00[ASN][1000 genomes]
rs72666625	1.00[ASN][1000 genomes]
rs72666629	1.00[ASN][1000 genomes]
rs72666633	1.00[ASN][1000 genomes]
rs72666638	1.00[ASN][1000 genomes]
rs72666642	1.00[ASN][1000 genomes]
rs72666643	1.00[ASN][1000 genomes]
rs73699303	1.00[ASN][1000 genomes]
rs7839115	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831406	chr8:99290745-99482076	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 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	chr8:99310200-99324200	Weak transcription	Fetal Heart	heart
2	chr8:99318800-99335200	Weak transcription	HSMM	muscle
3	chr8:99321600-99324600	Enhancers	Stomach Mucosa	stomach
4	chr8:99321600-99325200	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr8:99322800-99325600	Enhancers	HMEC	breast
6	chr8:99323000-99326000	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr8:99323200-99324000	Enhancers	Esophagus	oesophagus
8	chr8:99323200-99324200	Enhancers	Colonic Mucosa	Colon
9	chr8:99323200-99324400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr8:99323200-99324600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:99323200-99325400	Enhancers	NHEK	skin
12	chr8:99323800-99324000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum

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