Variant report

Variant	rs8017657
Chromosome Location	chr14:32845774-32845775
allele	A/G
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	chr14:32836600-32846800	Weak transcription	Fetal Brain Male	brain
2	chr14:32843400-32846600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr14:32843600-32846000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:32843600-32846200	Weak transcription	Brain Angular Gyrus	brain
5	chr14:32843600-32846600	Weak transcription	Brain Anterior Caudate	brain
6	chr14:32843600-32848600	Weak transcription	K562	blood
7	chr14:32843800-32846200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr14:32843800-32846400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr14:32843800-32848400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr14:32843800-32849000	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr14:32844000-32846200	Weak transcription	Brain Substantia Nigra	brain
12	chr14:32845200-32851000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr14:32845400-32846800	Weak transcription	HMEC	breast
14	chr14:32845400-32847200	Enhancers	Brain Hippocampus Middle	brain
15	chr14:32845400-32847800	Enhancers	Brain Cingulate Gyrus	brain
16	chr14:32845400-32848600	Weak transcription	NHEK	skin
17	chr14:32845600-32848600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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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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