Variant report

Variant	rs2285003
Chromosome Location	chr14:65283077-65283078
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65262000-65289800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:65268400-65290200	Weak transcription	Brain Germinal Matrix	brain
3	chr14:65271400-65289800	Weak transcription	Brain Anterior Caudate	brain
4	chr14:65273800-65287200	Weak transcription	K562	blood
5	chr14:65274600-65284600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr14:65275800-65290000	Weak transcription	Psoas Muscle	Psoas
7	chr14:65279400-65284200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr14:65279400-65284400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr14:65279400-65284400	Weak transcription	Aorta	Aorta
10	chr14:65279400-65284600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:65279400-65287000	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr14:65280800-65283400	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr14:65281600-65284000	Enhancers	Left Ventricle	heart
14	chr14:65281800-65283600	Enhancers	Right Ventricle	heart
15	chr14:65281800-65288400	Genic enhancers	Skeletal Muscle Female	skeletal muscle
16	chr14:65282800-65284200	Strong transcription	Fetal Muscle Leg	muscle
17	chr14:65283000-65283600	Enhancers	Fetal Heart	heart

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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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