Variant report

Variant rs12981573
Chromosome Location chr19:35899928-35899929
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:35894600-35900200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
2 chr19:35894800-35901000 Weak transcription Right Ventricle heart
3 chr19:35896600-35900000 Weak transcription Placenta Amnion Placenta Amnion
4 chr19:35899000-35900000 Enhancers Primary B cells from cord blood blood
5 chr19:35899000-35906200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr19:35899000-35907400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr19:35899200-35900200 Enhancers Primary neutrophils fromperipheralblood blood
8 chr19:35899200-35900200 Enhancers Primary B cells from peripheral blood blood
9 chr19:35899200-35900400 Enhancers Spleen Spleen
10 chr19:35899400-35900600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr19:35899400-35901400 Flanking Active TSS GM12878-XiMat blood

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