Variant report

Variant	rs59608717
Chromosome Location	chr12:43373142-43373143
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:43368600-43379200	Weak transcription	Fetal Heart	heart
2	chr12:43370600-43375200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr12:43371200-43373200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:43371600-43374800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr12:43371800-43373400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr12:43372000-43375200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr12:43372000-43375400	Weak transcription	HUVEC	blood vessel
8	chr12:43372200-43376800	Weak transcription	NHDF-Ad	bronchial
9	chr12:43372400-43374800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr12:43372600-43375200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr12:43372800-43375800	Enhancers	HSMM	muscle
12	chr12:43373000-43373200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr12:43373000-43373200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr12:43373000-43374000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:43373000-43374400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr12:43373000-43377400	Enhancers	HSMMtube	muscle

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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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