Variant report

Variant	rs12207248
Chromosome Location	chr2:229942382-229942383
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:229929000-229948400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr2:229931600-229945000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr2:229932000-229952800	Weak transcription	Stomach Smooth Muscle	stomach
4	chr2:229932400-229944600	Weak transcription	Aorta	Aorta
5	chr2:229933400-229952000	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr2:229936200-229946200	Weak transcription	HSMMtube	muscle
7	chr2:229936600-229947000	Weak transcription	HSMM	muscle
8	chr2:229940600-229952000	Weak transcription	Ovary	ovary
9	chr2:229940800-229947000	Weak transcription	Adipose Nuclei	Adipose
10	chr2:229940800-229953200	Weak transcription	Fetal Lung	lung
11	chr2:229941000-229942800	Weak transcription	Liver	Liver
12	chr2:229941000-229951400	Weak transcription	Left Ventricle	heart
13	chr2:229941200-229942600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr2:229942200-229948000	Weak transcription	Rectal Mucosa Donor 29	rectum

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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