Variant report

Variant rs189022477
Chromosome Location chr1:146983395-146983396
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:146978200-146987400 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr1:146978200-146987400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr1:146978400-146987200 Weak transcription Fetal Kidney kidney
4 chr1:146979800-146989400 Weak transcription Aorta Aorta
5 chr1:146981200-146987400 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr1:146981400-146983400 Enhancers Fetal Lung lung
7 chr1:146981600-146984000 Enhancers Liver Liver
8 chr1:146982200-146983600 Weak transcription HUES48 Cell Line embryonic stem cell
9 chr1:146982200-146985800 Weak transcription Hela-S3 cervix
10 chr1:146982200-146987400 Weak transcription Cortex derived primary cultured neurospheres brain
11 chr1:146982400-146987200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr1:146982400-146988600 Weak transcription Placenta Placenta
13 chr1:146983000-146985800 Weak transcription Right Atrium heart
14 chr1:146983000-146986000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr1:146983000-146987400 Weak transcription iPS-15b Cell Line embryonic stem cell
16 chr1:146983000-146987400 Weak transcription Left Ventricle heart
17 chr1:146983200-146983400 Flanking Active TSS Fetal Heart heart
18 chr1:146983200-146983800 Weak transcription iPS-20b Cell Line embryonic stem cell

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