Variant report

Variant	rs555012483
Chromosome Location	chr2:144535099-144535100
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	esv3447199	chr2:144534976-144535222	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:144529800-144535600	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr2:144530200-144535600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:144532600-144536200	Enhancers	Fetal Lung	lung
4	chr2:144534000-144536000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr2:144534000-144536400	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr2:144534800-144535200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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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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