Variant report

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3317742	chr18:45092079-45093413	Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv3317743	chr18:45092150-45093325	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:45089800-45094000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr18:45090200-45103000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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