Variant report

Variant	rs12633778
Chromosome Location	chr3:140936134-140936135
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:140931800-140941200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr3:140934400-140938400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr3:140935000-140937000	Enhancers	HepG2	liver
4	chr3:140935200-140936400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:140935800-140936200	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr3:140935800-140937800	Enhancers	Fetal Intestine Large	intestine
7	chr3:140935800-140938800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr3:140936000-140936400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr3:140936000-140936400	Enhancers	Fetal Intestine Small	intestine
10	chr3:140936000-140936600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr3:140936000-140937400	Enhancers	Psoas Muscle	Psoas
12	chr3:140936000-140937600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
13	chr3:140936000-140937800	Enhancers	Primary B cells from cord blood	blood

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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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