Variant report

Variant	rs35879668
Chromosome Location	chr7:116913320-116913321
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11973869	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13226446	0.82[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs34109572	1.00[EUR][1000 genomes]
rs34223626	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34422456	1.00[EUR][1000 genomes]
rs34507244	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs34678814	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs35131627	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35284736	0.81[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs35880748	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4256537	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6948009	1.00[EUR][1000 genomes]
rs71564590	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs71564591	0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831108	chr7:116749534-116952011	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:116909600-116920400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr7:116910800-116915000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:116911000-116913600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr7:116911200-116913600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:116911200-116915000	Weak transcription	NHLF	lung
6	chr7:116912000-116915000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:116912200-116915200	Weak transcription	Osteobl	bone
8	chr7:116912400-116914800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr7:116913000-116915000	Weak transcription	NHDF-Ad	bronchial
10	chr7:116913200-116913400	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr7:116913200-116913600	Enhancers	Fetal Kidney	kidney
12	chr7:116913200-116913800	Enhancers	NHEK	skin
13	chr7:116913200-116915200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr7:116913200-116915200	Enhancers	HMEC	breast

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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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