Variant report

Variant	rs57949951
Chromosome Location	chr10:22742789-22742790
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22739000-22743000	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr10:22740400-22743200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:22742200-22743400	Enhancers	Fetal Muscle Leg	muscle
4	chr10:22742400-22743000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr10:22742400-22743600	Enhancers	Fetal Heart	heart
6	chr10:22742400-22743800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr10:22742600-22743400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:22742600-22743400	Enhancers	Fetal Lung	lung
9	chr10:22742600-22743600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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