Variant report

Variant rs12572659
Chromosome Location chr10:18425999-18426000
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18423800-18426400 Enhancers iPS-15b Cell Line embryonic stem cell
2 chr10:18424200-18428800 Weak transcription H9 Cell Line embryonic stem cell
3 chr10:18425000-18428600 Weak transcription Colon Smooth Muscle Colon
4 chr10:18425000-18428600 Weak transcription Fetal Heart heart
5 chr10:18425200-18428600 Weak transcription Rectal Smooth Muscle rectum
6 chr10:18425400-18428400 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr10:18425600-18426000 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr10:18425600-18426000 Enhancers Cortex derived primary cultured neurospheres brain
9 chr10:18425600-18426000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr10:18425600-18426400 Enhancers HUES6 Cell Line embryonic stem cell
11 chr10:18425600-18426400 Enhancers iPS-20b Cell Line embryonic stem cell
12 chr10:18425600-18426600 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr10:18425600-18428800 Weak transcription Brain Anterior Caudate brain
14 chr10:18425800-18426400 Enhancers HUES64 Cell Line embryonic stem cell
15 chr10:18425800-18428600 Weak transcription Brain Substantia Nigra brain
16 chr10:18425800-18429000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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