Variant report

Variant	rs10953947
Chromosome Location	chr7:121404350-121404351
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10488054	0.83[EUR][1000 genomes]
rs10953941	0.80[EUR][1000 genomes]
rs10953943	0.80[EUR][1000 genomes]
rs10953944	0.83[EUR][1000 genomes]
rs10953946	0.83[EUR][1000 genomes]
rs12536101	0.83[EUR][1000 genomes]
rs12539525	0.80[EUR][1000 genomes]
rs12668960	0.83[EUR][1000 genomes]
rs12673165	0.82[EUR][1000 genomes]
rs1476925	0.83[EUR][1000 genomes]
rs1476926	0.83[EUR][1000 genomes]
rs17143719	0.80[EUR][1000 genomes]
rs17143727	0.82[EUR][1000 genomes]
rs55640247	0.80[EUR][1000 genomes]
rs55777148	0.83[EUR][1000 genomes]
rs59483937	0.83[EUR][1000 genomes]
rs62475665	0.83[EUR][1000 genomes]
rs62475691	0.83[EUR][1000 genomes]
rs62475692	0.83[EUR][1000 genomes]
rs62475693	0.83[EUR][1000 genomes]
rs62475694	0.83[EUR][1000 genomes]
rs6975770	0.80[EUR][1000 genomes]
rs7457523	0.83[EUR][1000 genomes]
rs7806895	0.83[EUR][1000 genomes]
rs9640803	0.83[EUR][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	nsv1032054	chr7:120926379-121432971	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv539103	chr7:120926379-121432971	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv429808	chr7:121384049-121600049	Weak transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:121395000-121406600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr7:121401200-121434000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	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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