Variant report

Variant	rs12086679
Chromosome Location	chr1:216881652-216881653
allele	A/G
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	chr1:216868200-216894000	Weak transcription	Placenta	Placenta
2	chr1:216879400-216883200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr1:216879400-216888400	Weak transcription	Gastric	stomach
4	chr1:216879600-216883400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:216879600-216883400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr1:216879800-216881800	Weak transcription	Fetal Heart	heart
7	chr1:216880000-216883400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr1:216880600-216883200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr1:216880800-216882000	Weak transcription	HUES64 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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