Variant report

Variant	rs2945568
Chromosome Location	chr8:96029432-96029433
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs2599717	1.00[AFR][1000 genomes]
rs2678824	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2678830	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2945567	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs538963	1.00[AFR][1000 genomes];1.00[AMR][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	nsv1017301	chr8:95273503-96248352	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	nsv539680	chr8:95273503-96248352	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv508520	chr8:95939373-96140068	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	35 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:96003200-96032600	Weak transcription	Gastric	stomach
2	chr8:96009000-96036400	Weak transcription	Spleen	Spleen
3	chr8:96023200-96030200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr8:96023400-96032600	Weak transcription	Right Atrium	heart
5	chr8:96023400-96036600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:96024800-96036400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr8:96026400-96033600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr8:96026800-96032600	Weak transcription	Left Ventricle	heart
9	chr8:96026800-96036400	Weak transcription	HMEC	breast
10	chr8:96029000-96030600	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr8:96029400-96029600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr8:96029400-96029600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr8:96029400-96029600	Enhancers	Esophagus	oesophagus
14	chr8:96029400-96029600	Enhancers	Right Ventricle	heart
15	chr8:96029400-96029800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr8:96029400-96029800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr8:96029400-96033200	Enhancers	Monocytes-CD14+_RO01746	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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