Variant report

Variant	rs9425561
Chromosome Location	chr1:172307571-172307572
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:172275200-172309800	Weak transcription	Left Ventricle	heart
2	chr1:172304000-172312200	Weak transcription	Aorta	Aorta
3	chr1:172307400-172307800	Enhancers	Primary B cells from peripheral blood	blood
4	chr1:172307400-172307800	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr1:172307400-172307800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:172307400-172308000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr1:172307400-172308000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr1:172307400-172308600	Flanking Active TSS	GM12878-XiMat	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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