Variant report

Variant	rs566142613
Chromosome Location	chr6:71868275-71868276
allele	A/G
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	nsv527265	chr6:71867477-71902656	Enhancers Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71866400-71869800	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr6:71866600-71868400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:71866600-71869800	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr6:71866800-71868400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr6:71866800-71868400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr6:71866800-71870000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:71867000-71868600	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr6:71867200-71869800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr6:71867400-71868600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr6:71867400-71868800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:71867600-71868600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr6:71868000-71869400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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