Variant report

Variant	rs146105238
Chromosome Location	chr6:44494215-44494216
allele	-/AT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv969300	chr6:44493755-44494845	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44492400-44496600	Enhancers	Fetal Thymus	thymus
2	chr6:44492400-44509800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr6:44493000-44494600	Weak transcription	Thymus	Thymus
4	chr6:44493200-44494400	Weak transcription	Dnd41	blood
5	chr6:44493200-44498000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr6:44493400-44494800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:44493600-44495600	Weak transcription	iPS DF 19.11 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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