Variant report

Variant	rs556438664
Chromosome Location	chr1:217121054-217121055
allele	C/T
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	esv3445404	chr1:217120745-217121066	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217111000-217125400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:217117800-217121200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr1:217118800-217125400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr1:217119600-217125400	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr1:217119600-217125400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr1:217119800-217126000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr1:217120400-217126200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr1:217120800-217121200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr1:217121000-217121400	Enhancers	iPS-15b 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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