Variant report

Variant	rs577495633
Chromosome Location	chr11:119659996-119659997
allele	G/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	nsv528824	chr11:119650105-119661809	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	esv1837528	chr11:119659918-119666352	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:119657200-119663600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr11:119658000-119661400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr11:119658000-119662400	Weak transcription	Fetal Brain Female	brain
4	chr11:119658400-119660400	Weak transcription	Fetal Brain Male	brain
5	chr11:119659200-119662400	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
6	chr11:119659200-119662800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr11:119659800-119660400	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
8	chr11:119659800-119660600	Enhancers	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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