Variant report

Variant	rs9958056
Chromosome Location	chr18:44127225-44127226
allele	C/T
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	chr18:44126600-44127800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr18:44126600-44128000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr18:44126600-44128200	Weak transcription	Fetal Stomach	stomach
4	chr18:44126600-44128800	Weak transcription	Colon Smooth Muscle	Colon
5	chr18:44126600-44130400	Weak transcription	Right Atrium	heart
6	chr18:44126600-44130600	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr18:44126600-44130600	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr18:44126600-44130800	Weak transcription	Spleen	Spleen
9	chr18:44126600-44131200	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr18:44126600-44132200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr18:44126600-44133800	Weak transcription	Brain Hippocampus Middle	brain
12	chr18:44126600-44133800	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr18:44126600-44134000	Weak transcription	Brain Angular Gyrus	brain
14	chr18:44126600-44135000	Weak transcription	Brain Cingulate Gyrus	brain
15	chr18:44126600-44137200	Weak transcription	Primary monocytes fromperipheralblood	blood
16	chr18:44126600-44139200	Weak transcription	Lung	lung
17	chr18:44126600-44143000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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