Variant report

Variant	rs6957595
Chromosome Location	chr7:80769467-80769468
allele	A/T
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:15)

rs_ID	r²[population]
rs10264882	0.93[ASN][1000 genomes]
rs10272094	0.88[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13228254	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13242185	0.93[ASN][1000 genomes]
rs1605917	0.93[ASN][1000 genomes]
rs17616148	0.93[ASN][1000 genomes]
rs1859678	0.93[ASN][1000 genomes]
rs34252288	0.93[ASN][1000 genomes]
rs35141375	0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs56034302	0.93[ASN][1000 genomes]
rs62467422	0.93[ASN][1000 genomes]
rs6467590	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6956639	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7779992	0.93[ASN][1000 genomes]
rs7795202	0.86[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	nsv1034690	chr7:80520004-80987682	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv888556	chr7:80695828-80797794	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv831044	chr7:80721773-80918591	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 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	chr7:80763200-80780200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr7:80767800-80769800	Enhancers	Monocytes-CD14+_RO01746	blood
3	chr7:80768000-80770200	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr7:80768000-80771000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:80768200-80770800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:80768200-80771000	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr7:80768200-80771000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:80768600-80770400	Enhancers	Fetal Lung	lung
9	chr7:80768800-80770600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr7:80768800-80771000	Enhancers	Primary hematopoietic stem cells	blood
11	chr7:80769000-80771400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr7:80769200-80770800	Enhancers	HepG2	liver

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