Variant report

Variant rs3899908
Chromosome Location chr10:18766640-18766641
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18732400-18801600 Weak transcription Pancreas Pancrea
2 chr10:18753000-18775600 Weak transcription Right Atrium heart
3 chr10:18761800-18766800 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr10:18762200-18769600 Enhancers Fetal Heart heart
5 chr10:18763600-18767400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr10:18763600-18778400 Weak transcription Stomach Smooth Muscle stomach
7 chr10:18764800-18767800 Enhancers Cortex derived primary cultured neurospheres brain
8 chr10:18765400-18767400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
9 chr10:18765400-18767600 Enhancers iPS-15b Cell Line embryonic stem cell
10 chr10:18765800-18771400 Weak transcription Left Ventricle heart
11 chr10:18766600-18766800 Enhancers H9 Cell Line embryonic stem cell
12 chr10:18766600-18767000 Weak transcription iPS-20b Cell Line embryonic stem cell

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