Variant report

Variant	rs28468649
Chromosome Location	chr8:125042001-125042002
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124971800-125052000	Weak transcription	Gastric	stomach
2	chr8:125031000-125048600	Weak transcription	Stomach Mucosa	stomach
3	chr8:125035600-125042600	Weak transcription	Primary hematopoietic stem cells	blood
4	chr8:125037000-125045600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:125040200-125042600	Weak transcription	Psoas Muscle	Psoas
6	chr8:125040600-125045400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr8:125040600-125045600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr8:125040800-125043600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr8:125040800-125045200	Weak transcription	Fetal Heart	heart
10	chr8:125041000-125042600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr8:125041000-125043000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:125041000-125046200	Weak transcription	Fetal Muscle Leg	muscle
13	chr8:125041000-125048400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr8:125041800-125042600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:125042000-125044400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

Quick Search:

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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