Variant report

Variant	rs73256773
Chromosome Location	chr14:32828724-32828725
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:32797200-32831600	Weak transcription	Right Atrium	heart
2	chr14:32819200-32834200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr14:32822400-32834400	Weak transcription	Fetal Brain Female	brain
4	chr14:32826000-32829000	Enhancers	Brain Hippocampus Middle	brain
5	chr14:32828000-32835200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr14:32828200-32830600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr14:32828200-32830600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr14:32828200-32830600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr14:32828200-32831000	Weak transcription	Brain Angular Gyrus	brain
10	chr14:32828200-32831800	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr14:32828200-32833400	Weak transcription	Brain Germinal Matrix	brain
12	chr14:32828400-32830400	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr14:32828400-32830400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr14:32828400-32830400	Weak transcription	Brain Anterior Caudate	brain
15	chr14:32828400-32830400	Weak transcription	Brain Substantia Nigra	brain

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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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