Variant report

Variant	rs12274428
Chromosome Location	chr11:45258629-45258630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:45239800-45265400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:45248800-45274200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr11:45249800-45273800	Weak transcription	Spleen	Spleen
4	chr11:45250800-45259200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:45252600-45264600	Weak transcription	Fetal Intestine Large	intestine
6	chr11:45254800-45259400	Weak transcription	Fetal Brain Female	brain
7	chr11:45255400-45259400	Weak transcription	Fetal Brain Male	brain
8	chr11:45255800-45273800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr11:45256200-45259000	Weak transcription	Fetal Stomach	stomach
10	chr11:45257000-45264600	Weak transcription	Fetal Intestine Small	intestine
11	chr11:45257800-45259200	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr11:45258400-45260000	Enhancers	Brain Dorsolateral Prefrontal Cortex	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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