Variant report

Variant	rs567298181
Chromosome Location	chr11:119767718-119767719
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1051526	chr11:119750335-119775811	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1038232	chr11:119759344-119785065	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1044698	chr11:119767614-119789683	Enhancers Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119747200-119768200	Weak transcription	Fetal Intestine Small	intestine
2	chr11:119763000-119767800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr11:119763000-119768400	Weak transcription	Left Ventricle	heart
4	chr11:119763000-119780800	Weak transcription	Right Atrium	heart
5	chr11:119764000-119768000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:119764600-119768000	Weak transcription	Fetal Heart	heart
7	chr11:119765800-119768600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:119765800-119773800	Weak transcription	Esophagus	oesophagus
9	chr11:119766400-119768200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr11:119766400-119768200	Weak transcription	Placenta	Placenta
11	chr11:119767200-119768000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr11:119767400-119767800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:119767400-119768600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:119767400-119769000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr11:119767600-119769200	Enhancers	Stomach Smooth Muscle	stomach

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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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