Variant report

Variant	rs1901247
Chromosome Location	chr7:138466161-138466162
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs28503872	1.00[EUR][1000 genomes]
rs58440371	1.00[EUR][1000 genomes]
rs60569142	1.00[EUR][1000 genomes]
rs6956608	1.00[EUR][1000 genomes]
rs6976485	1.00[EUR][1000 genomes]
rs73459207	1.00[EUR][1000 genomes]
rs73729926	1.00[AMR][1000 genomes]
rs73730411	1.00[EUR][1000 genomes]
rs73730416	1.00[EUR][1000 genomes]
rs73730418	1.00[EUR][1000 genomes]
rs73730423	1.00[EUR][1000 genomes]
rs73730424	1.00[EUR][1000 genomes]
rs73730425	1.00[EUR][1000 genomes]
rs73730427	1.00[EUR][1000 genomes]
rs7790139	1.00[EUR][1000 genomes]
rs9692528	1.00[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	nsv1030956	chr7:138163169-138579519	Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:138461400-138470400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:138464000-138470600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:138465400-138469600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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