Variant report

Variant	rs560843572
Chromosome Location	chr5:68332099-68332100
allele	-/TTG
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	esv3374365	chr5:68331863-68332122	Enhancers Weak transcription	Chromatin interactive region	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	chr5:68330600-68339000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:68331200-68332400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:68331600-68332200	Enhancers	HMEC	breast
4	chr5:68331600-68332400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr5:68331600-68332400	Enhancers	NHEK	skin
6	chr5:68332000-68332800	Weak transcription	K562	blood

Quick Search:

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

what's new

Quick links