Variant report

Variant	rs9425565
Chromosome Location	chr1:172309690-172309691
allele	C/T
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	chr1:172275200-172309800	Weak transcription	Left Ventricle	heart
2	chr1:172304000-172312200	Weak transcription	Aorta	Aorta
3	chr1:172307600-172312600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr1:172307800-172312200	Weak transcription	Primary T helper cells fromperipheralblood	blood
5	chr1:172307800-172312200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr1:172308000-172311800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
7	chr1:172308000-172312000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:172308000-172312000	Weak transcription	A549	lung
9	chr1:172308000-172312200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:172308000-172312200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr1:172308000-172312400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr1:172308000-172313200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr1:172308600-172311400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr1:172309000-172310000	Flanking Active TSS	GM12878-XiMat	blood
15	chr1:172309200-172313800	Enhancers	Primary B cells from peripheral blood	blood
16	chr1:172309400-172309800	Enhancers	Primary monocytes fromperipheralblood	blood
17	chr1:172309600-172309800	Enhancers	Brain Hippocampus Middle	brain

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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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