Variant report

Variant	rs1508564
Chromosome Location	chr8:118694595-118694596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1508565	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16890085	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17753209	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17753221	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17753372	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17753630	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs17815416	1.00[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs17815428	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17815452	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17815523	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17815657	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs17815776	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs2136106	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4490876	1.00[AFR][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	nsv1019636	chr8:118598433-118946091	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv539734	chr8:118598433-118946091	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv831438	chr8:118679896-118823600	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv891410	chr8:118684994-118730344	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	1 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	chr8:118689200-118698200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:118689200-118698600	Weak transcription	HMEC	breast
3	chr8:118689200-118718600	Weak transcription	Osteobl	bone
4	chr8:118689400-118695200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr8:118690800-118701400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr8:118692400-118714400	Weak transcription	HSMM	muscle
7	chr8:118693000-118698400	Weak transcription	NHEK	skin
8	chr8:118693600-118694600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:118694200-118694600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:118694200-118694600	Enhancers	HSMMtube	muscle
11	chr8:118694200-118694600	Enhancers	NHLF	lung
12	chr8:118694200-118694800	Enhancers	NHDF-Ad	bronchial

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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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