Variant report

Variant	rs114270872
Chromosome Location	chr7:105223093-105223094
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
EFCAB10	TF binding region
ENSG00000130255	Chromatin interaction
ENSG00000091127	Chromatin interaction
ENSG00000135249	Chromatin interaction

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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	nsv981568	chr7:105222012-105223485	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:105222000-105229800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
2	chr7:105222200-105229800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr7:105222200-105253000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:105222400-105225400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr7:105222800-105237000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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