Variant report

Variant	rs34919348
Chromosome Location	chr2:115698285-115698286
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:115695400-115698800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr2:115697600-115699400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr2:115697800-115699000	Enhancers	Brain Angular Gyrus	brain
4	chr2:115697800-115699000	Enhancers	Brain Cingulate Gyrus	brain
5	chr2:115697800-115699000	Enhancers	Brain Substantia Nigra	brain
6	chr2:115697800-115699400	Enhancers	Brain Inferior Temporal Lobe	brain
7	chr2:115698200-115698600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:115698200-115698800	Enhancers	Brain Germinal Matrix	brain
9	chr2:115698200-115699400	Enhancers	Brain Hippocampus Middle	brain

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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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