Variant report

Variant	rs187449874
Chromosome Location	chr1:85204880-85204881
allele	A/C
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	esv3413749	chr1:85203614-85205762	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85204200-85205000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr1:85204200-85205400	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr1:85204200-85212800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr1:85204200-85230400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr1:85204400-85205600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr1:85204800-85206400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr1:85204800-85206600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr1:85204800-85206800	Enhancers	iPS-18 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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