Variant report

Variant	rs111316991
Chromosome Location	chr5:91494994-91494995
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	nsv882376	chr5:91367222-91525968	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv882377	chr5:91441015-91502103	Active TSS Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv882378	chr5:91477046-91601492	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:91494800-91495200	Active TSS	H9 Cell Line	embryonic stem cell
2	chr5:91494800-91495400	Active TSS	iPS-15b Cell Line	embryonic stem cell
3	chr5:91494800-91495400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr5:91494800-91495400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr5:91494800-91495600	Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr5:91494800-91496000	Active TSS	HUES6 Cell Line	embryonic stem cell

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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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