Variant report

Variant	rs568334885
Chromosome Location	chr2:31319112-31319113
allele	C/T
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	nsv948552	chr2:31118599-31595424	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	esv3437289	chr2:31318966-31319295	Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:31302000-31321400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr2:31302600-31325200	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr2:31307400-31331600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr2:31310600-31320800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr2:31310600-31346800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:31313000-31321000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr2:31314800-31320800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr2:31316000-31320400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr2:31318200-31320400	Weak transcription	NHEK	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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