Variant report

Variant	rs73204026
Chromosome Location	chr12:116834127-116834128
allele	C/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	chr12:116830200-116835000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr12:116830200-116843800	Weak transcription	NHLF	lung
3	chr12:116830400-116834800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:116830400-116834800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr12:116830400-116836000	Weak transcription	NHDF-Ad	bronchial
6	chr12:116832000-116835600	Weak transcription	Primary T cells from cord blood	blood
7	chr12:116832400-116836000	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr12:116833600-116834800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr12:116833800-116844200	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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