Variant report

Variant	rs12250744
Chromosome Location	chr10:94572022-94572023
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:94571000-94574400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr10:94571200-94574600	Weak transcription	K562	blood
3	chr10:94571400-94572600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:94571400-94572600	Enhancers	HUVEC	blood vessel
5	chr10:94571600-94572200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr10:94571600-94572400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr10:94571600-94572400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr10:94571800-94572200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr10:94571800-94572200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr10:94571800-94572400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr10:94571800-94572600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr10:94572000-94575400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

Quick Search:

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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