Variant report

Variant	rs9918358
Chromosome Location	chr6:12540285-12540286
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12537600-12540400	Enhancers	HUVEC	blood vessel
2	chr6:12537800-12545200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:12538000-12546200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr6:12539400-12544600	Weak transcription	Aorta	Aorta
5	chr6:12539600-12540600	Weak transcription	NH-A	brain
6	chr6:12539600-12543800	Weak transcription	Duodenum Mucosa	Duodenum
7	chr6:12539600-12544000	Weak transcription	Stomach Mucosa	stomach
8	chr6:12539600-12545200	Weak transcription	Osteobl	bone
9	chr6:12540000-12543800	Weak transcription	Fetal Intestine Small	intestine
10	chr6:12540200-12543800	Weak transcription	Fetal Intestine Large	intestine

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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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