Variant report

Variant	rs200896633
Chromosome Location	chr3:22975930-22975931
allele	-/AC
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1014828	chr3:22554271-23033498	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1008306	chr3:22762892-23026548	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv3364617	chr3:22975148-22978146	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a
4	esv3354179	chr3:22975448-22976696	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:22970200-22976600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr3:22970600-22976400	Weak transcription	Fetal Muscle Leg	muscle
3	chr3:22971000-22976200	Weak transcription	Fetal Stomach	stomach
4	chr3:22971000-22978400	Weak transcription	Stomach Smooth Muscle	stomach
5	chr3:22971000-22978800	Weak transcription	Colon Smooth Muscle	Colon
6	chr3:22971200-22979000	Weak transcription	Ovary	ovary
7	chr3:22975600-22976000	Weak transcription	Fetal Lung	lung

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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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