Variant report

Variant	rs1844927
Chromosome Location	chr3:111756435-111756436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111754400-111762600	Weak transcription	Fetal Heart	heart
2	chr3:111754600-111756800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:111754600-111758200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:111755000-111757600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr3:111756200-111763200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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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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