Variant report

Variant	rs376363321
Chromosome Location	chr18:40161282-40161283
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	esv3447158	chr18:40045478-40320720	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv2754458	chr18:40070202-40164902	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	esv1822969	chr18:40161230-40164937	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:40160800-40162400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr18:40160800-40163400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr18:40160800-40166400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr18:40161200-40161400	Enhancers	H9 Cell Line	embryonic stem cell
5	chr18:40161200-40162200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr18:40161200-40162400	Enhancers	HUES64 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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