Variant report

Variant	rs572956913
Chromosome Location	chr6:121801043-121801044
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv966657	chr6:121786080-121806494	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv5458	chr6:121787521-121823054	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr6:121800600-121801200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:121800600-121801200	Enhancers	Placenta	Placenta
3	chr6:121800800-121801800	Active TSS	A549	lung
4	chr6:121800800-121802000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr6:121801000-121801200	Enhancers	Placenta Amnion	Placenta Amnion
6	chr6:121801000-121801200	Enhancers	Hela-S3	cervix
7	chr6:121801000-121801600	Enhancers	HUES6 Cell Line	embryonic stem cell
8	chr6:121801000-121803200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr6:121801000-121806200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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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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