Variant report

Variant rs4462708
Chromosome Location chr19:56833791-56833792
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr19:56827600-56835400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr19:56829000-56837000 Enhancers Primary monocytes fromperipheralblood blood
3 chr19:56829200-56834200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
4 chr19:56829800-56834000 Enhancers Primary hematopoietic stem cells blood
5 chr19:56829800-56834200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr19:56832200-56833800 Enhancers Primary B cells from cord blood blood
7 chr19:56832200-56834000 Enhancers Right Atrium heart
8 chr19:56832200-56834200 Flanking Active TSS K562 blood
9 chr19:56832600-56834000 Enhancers Fetal Heart heart
10 chr19:56832800-56834000 Enhancers Primary B cells from peripheral blood blood
11 chr19:56833200-56833800 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr19:56833400-56833800 Flanking Active TSS Primary hematopoietic stem cells short term culture blood
13 chr19:56833600-56833800 Enhancers Left Ventricle heart

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