Variant report

Variant	rs2060145
Chromosome Location	chr8:129807905-129807906
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129784000-129809800	Weak transcription	Dnd41	blood
2	chr8:129805400-129808200	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr8:129806000-129808200	Enhancers	Fetal Muscle Leg	muscle
4	chr8:129806000-129808600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr8:129807000-129812200	Weak transcription	Fetal Intestine Small	intestine
6	chr8:129807000-129820800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr8:129807600-129811600	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr8:129807600-129812000	Weak transcription	Fetal Stomach	stomach

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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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