Variant report

Variant	rs61842434
Chromosome Location	chr10:18426435-18426436
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:18424200-18428800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr10:18425000-18428600	Weak transcription	Colon Smooth Muscle	Colon
3	chr10:18425000-18428600	Weak transcription	Fetal Heart	heart
4	chr10:18425200-18428600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr10:18425400-18428400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:18425600-18426600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr10:18425600-18428800	Weak transcription	Brain Anterior Caudate	brain
8	chr10:18425800-18428600	Weak transcription	Brain Substantia Nigra	brain
9	chr10:18425800-18429000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr10:18426000-18428400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr10:18426000-18428600	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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