Variant report

Variant	rs186790780
Chromosome Location	chr6:11635922-11635923
allele	A/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	esv2763532	chr6:11634722-11641048	Enhancers Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11633200-11636600	Weak transcription	Fetal Lung	lung
2	chr6:11633200-11636800	Weak transcription	Gastric	stomach
3	chr6:11633200-11640200	Weak transcription	Aorta	Aorta
4	chr6:11633400-11636800	Weak transcription	Lung	lung
5	chr6:11633600-11636600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr6:11633600-11637000	Weak transcription	NH-A	brain
7	chr6:11633600-11637200	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr6:11633600-11637200	Weak transcription	HSMM	muscle
9	chr6:11633600-11637400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:11633800-11637400	Weak transcription	HSMMtube	muscle
11	chr6:11634400-11636600	Weak transcription	Stomach Mucosa	stomach
12	chr6:11634800-11637400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:11635600-11638000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr6:11635800-11636200	Weak transcription	Pancreas	Pancrea

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