Variant report

Variant	rs6952769
Chromosome Location	chr7:107771850-107771851
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10487838	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10487840	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10953559	0.86[AFR][1000 genomes]
rs12666092	0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17155006	0.84[AFR][1000 genomes]
rs17155042	1.00[EUR][1000 genomes]
rs6466216	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73197625	1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73197627	0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73197628	1.00[EUR][1000 genomes];1.00[ASN][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	nsv1033979	chr7:107003734-107877761	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv949344	chr7:107396502-107987085	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv831089	chr7:107687618-107877240	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107767400-107772200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:107768800-107773000	Weak transcription	Placenta	Placenta
3	chr7:107769000-107772800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:107769000-107772800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:107769000-107773000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:107770200-107773000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:107771200-107772000	Enhancers	NHEK	skin
8	chr7:107771400-107772800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:107771400-107772800	Weak transcription	Fetal Kidney	kidney
10	chr7:107771400-107773000	Weak transcription	Esophagus	oesophagus
11	chr7:107771800-107772200	Weak transcription	HMEC	breast

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