Variant report

Variant	rs10237579
Chromosome Location	chr7:140924561-140924562
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:140903600-140934200	Weak transcription	Fetal Brain Female	brain
2	chr7:140904200-140925000	Weak transcription	Brain Anterior Caudate	brain
3	chr7:140904600-140933200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr7:140911000-140925600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr7:140914600-140937800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:140914800-140932400	Weak transcription	Brain Germinal Matrix	brain
7	chr7:140918200-140925800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr7:140919000-140925600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr7:140921400-140928400	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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