Variant report

Variant	rs11117683
Chromosome Location	chr1:216980277-216980278
allele	A/C
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	chr1:216978600-216980400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr1:216979000-216980400	Enhancers	Skeletal Muscle Male	skeletal muscle
3	chr1:216979000-216980400	Weak transcription	HSMMtube	muscle
4	chr1:216979000-216980600	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr1:216979000-216986200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:216979400-216980400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr1:216979400-216980600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr1:216979400-216983000	Weak transcription	Psoas Muscle	Psoas
9	chr1:216979600-216983200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr1:216979800-216985000	Weak transcription	Fetal Heart	heart
11	chr1:216979800-216985200	Weak transcription	Brain Substantia Nigra	brain
12	chr1:216979800-216988800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:216979800-216989000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr1:216980000-216984800	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr1:216980200-216986400	Weak transcription	Fetal Muscle Leg	muscle
16	chr1:216980200-216987400	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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