Variant report

Variant	rs3065417
Chromosome Location	chr21:39964281-39964282
allele	-/AG
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	esv3378727	chr21:39964137-39964474	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv186481	chr21:39964281-39964282	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	esv2062254	chr21:39964281-39964283	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:39955800-39971200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr21:39956600-39966000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr21:39963800-39964400	Enhancers	Fetal Muscle Leg	muscle
4	chr21:39964000-39964400	Enhancers	Fetal Muscle Trunk	muscle
5	chr21:39964000-39964400	Enhancers	Spleen	Spleen
6	chr21:39964200-39964600	Enhancers	Aorta	Aorta
7	chr21:39964200-39964800	Enhancers	Fetal Brain Female	brain

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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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