Variant report

Variant	rs16938191
Chromosome Location	chr11:45260786-45260787
allele	A/C
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	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	chr11:45252600-45264600	Weak transcription	Fetal Intestine Large	intestine
5	chr11:45255800-45273800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr11:45257000-45264600	Weak transcription	Fetal Intestine Small	intestine
7	chr11:45259000-45261200	Enhancers	Fetal Stomach	stomach
8	chr11:45259800-45261000	Enhancers	NH-A	brain
9	chr11:45259800-45279800	Weak transcription	Fetal Brain Male	brain
10	chr11:45260000-45260800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:45260000-45260800	Enhancers	Muscle Satellite Cultured Cells	--
12	chr11:45260000-45261000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr11:45260000-45261000	Enhancers	HSMMtube	muscle
14	chr11:45260000-45261200	Weak transcription	Fetal Brain Female	brain
15	chr11:45260000-45265800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr11:45260200-45260800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr11:45260200-45260800	Enhancers	Osteobl	bone

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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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