Variant report

Variant	rs376437022
Chromosome Location	chr2:211926418-211926419
allele	C/T
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	nsv1012193	chr2:211684524-212072213	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv875772	chr2:211893388-211946057	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv834521	chr2:211918881-212057872	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv963972	chr2:211922680-211928471	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211925600-211926600	Enhancers	Fetal Intestine Small	intestine
2	chr2:211926200-211926600	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr2:211926200-211927200	Enhancers	HepG2	liver
4	chr2:211926400-211927200	Enhancers	Liver	Liver
5	chr2:211926400-211927200	Enhancers	Fetal Intestine Large	intestine
6	chr2:211926400-211927400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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