Variant report

Variant	rs17056145
Chromosome Location	chr6:128953255-128953256
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11154445	0.89[ASN][1000 genomes]
rs12201837	0.93[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs1341590	0.89[ASN][1000 genomes]
rs1341591	0.89[ASN][1000 genomes]
rs1341592	0.92[ASN][1000 genomes]
rs1341593	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2153706	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs2153707	0.92[ASN][1000 genomes]
rs3822946	0.98[ASN][1000 genomes]
rs6569539	0.89[ASN][1000 genomes]
rs6909897	1.00[CHB][hapmap];0.87[JPT][hapmap];0.97[ASN][1000 genomes]
rs9372897	0.98[ASN][1000 genomes]
rs9372898	0.98[ASN][1000 genomes]
rs9375582	0.98[ASN][1000 genomes]
rs9375583	0.89[ASN][1000 genomes]
rs9375584	0.89[ASN][1000 genomes]
rs9492031	0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs969970	0.94[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs981598	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[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	nsv1020071	chr6:128579774-129048919	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv538441	chr6:128579774-129048919	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv830801	chr6:128878436-129064667	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:128951000-128953800	Enhancers	HMEC	breast
2	chr6:128951600-128953400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:128952400-128962200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:128952800-128954000	Enhancers	NHEK	skin
5	chr6:128953000-128953400	Weak transcription	Fetal Heart	heart
6	chr6:128953200-128953400	Enhancers	Pancreas	Pancrea
7	chr6:128953200-128953400	Enhancers	Stomach Mucosa	stomach
8	chr6:128953200-128953800	Enhancers	HepG2	liver
9	chr6:128953200-128954000	Enhancers	Hela-S3	cervix
10	chr6:128953200-128954400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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

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