Variant report

Variant	rs62649118
Chromosome Location	chr12:119513722-119513723
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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	nsv1047036	chr12:119477583-119992640	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
2	esv3327170	chr12:119511269-119515867	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv3432143	chr12:119513332-119513858	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	n/a

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:119510000-119519800	Weak transcription	Fetal Brain Female	brain
2	chr12:119513200-119513800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr12:119513200-119513800	ZNF genes & repeats	Pancreas	Pancrea
4	chr12:119513200-119514000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
5	chr12:119513200-119514000	ZNF genes & repeats	Fetal Kidney	kidney
6	chr12:119513400-119513800	ZNF genes & repeats	Fetal Brain Male	brain

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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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