Variant report

Variant	rs59084003
Chromosome Location	chr1:215154276-215154277
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:215141800-215162600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr1:215142000-215155800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr1:215152000-215156200	Weak transcription	HSMMtube	muscle
4	chr1:215153000-215155200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:215153000-215155600	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr1:215153000-215156400	Weak transcription	NHDF-Ad	bronchial
7	chr1:215153200-215155600	Weak transcription	Osteobl	bone

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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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