Variant report

Variant rs73340856
Chromosome Location chr21:16502464-16502465
allele A/C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:16494200-16502600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr21:16494400-16502800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr21:16499800-16502600 Weak transcription Fetal Muscle Leg muscle
4 chr21:16499800-16506400 Weak transcription Left Ventricle heart
5 chr21:16500400-16505800 Weak transcription Small Intestine intestine
6 chr21:16500600-16510800 Weak transcription Psoas Muscle Psoas
7 chr21:16500800-16505800 Weak transcription Duodenum Mucosa Duodenum
8 chr21:16501200-16506000 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr21:16501400-16505600 Weak transcription Primary monocytes fromperipheralblood blood
10 chr21:16501800-16506600 Weak transcription Primary B cells from peripheral blood blood
11 chr21:16502000-16503800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr21:16502000-16506200 Enhancers Primary hematopoietic stem cells blood
13 chr21:16502200-16503000 Enhancers NHEK skin
14 chr21:16502200-16506600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --

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