Variant report

Variant	rs73354909
Chromosome Location	chr10:89597868-89597869
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89592800-89603200	Weak transcription	Aorta	Aorta
2	chr10:89593400-89600800	Weak transcription	A549	lung
3	chr10:89597400-89600800	Weak transcription	Hela-S3	cervix
4	chr10:89597600-89599400	Weak transcription	Fetal Intestine Small	intestine
5	chr10:89597800-89599000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr10:89597800-89600200	Weak transcription	Fetal Intestine Large	intestine
7	chr10:89597800-89602200	Weak transcription	GM12878-XiMat	blood
8	chr10:89597800-89603000	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr10:89597800-89604000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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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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