Variant report

Variant	rs79564062
Chromosome Location	chr2:86619908-86619909
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3412938	chr2:86370969-86867936	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
2	esv18769	chr2:86619882-86620685	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:86615000-86620200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:86615800-86620200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr2:86619600-86620800	Enhancers	Left Ventricle	heart
4	chr2:86619600-86621200	Enhancers	Fetal Muscle Leg	muscle
5	chr2:86619600-86621600	Enhancers	Fetal Intestine Large	intestine
6	chr2:86619600-86622000	Enhancers	Fetal Intestine Small	intestine
7	chr2:86619800-86620400	Enhancers	Fetal Heart	heart
8	chr2:86619800-86621800	Enhancers	HSMMtube	muscle
9	chr2:86619800-86622800	Enhancers	Psoas Muscle	Psoas

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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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