Variant report

Variant	rs285482
Chromosome Location	chr1:165410723-165410724
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165398200-165412200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:165403800-165412400	Weak transcription	Brain Substantia Nigra	brain
3	chr1:165408400-165412400	Enhancers	Fetal Muscle Leg	muscle
4	chr1:165408600-165411600	Enhancers	Fetal Lung	lung
5	chr1:165409000-165411000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:165410000-165410800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:165410200-165411400	Enhancers	Brain Anterior Caudate	brain
8	chr1:165410200-165413000	Active TSS	Brain Germinal Matrix	brain
9	chr1:165410400-165411000	Enhancers	Psoas Muscle	Psoas
10	chr1:165410400-165411600	Enhancers	Lung	lung
11	chr1:165410400-165411800	Enhancers	Fetal Muscle Trunk	muscle
12	chr1:165410400-165412000	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr1:165410600-165410800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr1:165410600-165410800	Bivalent Enhancer	HSMMtube	muscle
15	chr1:165410600-165411000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
16	chr1:165410600-165411000	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr1:165410600-165411800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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