Variant report

Variant	rs61796872
Chromosome Location	chr3:178435152-178435153
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178417800-178436800	Weak transcription	Right Ventricle	heart
2	chr3:178432200-178436600	Weak transcription	Right Atrium	heart
3	chr3:178432800-178436200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:178432800-178436600	Weak transcription	Fetal Lung	lung
5	chr3:178433200-178436800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr3:178433400-178436600	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr3:178433400-178436800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr3:178433800-178436600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:178433800-178436600	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr3:178434000-178435600	Weak transcription	Fetal Heart	heart
11	chr3:178434000-178436800	Weak transcription	Fetal Muscle Leg	muscle
12	chr3:178434000-178436800	Weak transcription	HSMMtube	muscle
13	chr3:178434800-178436800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:178435000-178435200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr3:178435000-178435400	Enhancers	Left Ventricle	heart

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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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