Variant report

Variant	rs571215906
Chromosome Location	chr11:119768373-119768374
allele	A/G
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:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119763000-119768400	Weak transcription	Left Ventricle	heart
2	chr11:119763000-119780800	Weak transcription	Right Atrium	heart
3	chr11:119765800-119768600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
4	chr11:119765800-119773800	Weak transcription	Esophagus	oesophagus
5	chr11:119767400-119768600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:119767400-119769000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr11:119767600-119769200	Enhancers	Stomach Smooth Muscle	stomach
8	chr11:119767800-119768600	Enhancers	Aorta	Aorta
9	chr11:119767800-119768800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr11:119767800-119770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr11:119768000-119768600	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr11:119768000-119768800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr11:119768000-119768800	Bivalent Enhancer	Fetal Stomach	stomach
14	chr11:119768000-119769600	Enhancers	Fetal Heart	heart
15	chr11:119768000-119778000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:119768200-119768600	Enhancers	Fetal Intestine Small	intestine
17	chr11:119768200-119768600	Enhancers	Fetal Muscle Trunk	muscle
18	chr11:119768200-119768800	Enhancers	Placenta	Placenta

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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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