Variant report

Variant	rs73087022
Chromosome Location	chr5:35309903-35309904
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:35308200-35310400	Enhancers	Fetal Brain Female	brain
2	chr5:35308600-35310200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr5:35308600-35310400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr5:35308800-35310000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr5:35308800-35310000	Weak transcription	Brain Germinal Matrix	brain
6	chr5:35309000-35310000	Weak transcription	Fetal Brain Male	brain
7	chr5:35309000-35310000	Weak transcription	Pancreas	Pancrea
8	chr5:35309000-35311200	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr5:35309200-35310400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr5:35309200-35310400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr5:35309600-35312800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr5:35309800-35310000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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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