Variant report

Variant rs2002625
Chromosome Location chr21:16501314-16501315
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr21:16500200-16501400 Enhancers Primary monocytes fromperipheralblood blood
6 chr21:16500200-16501400 Enhancers Primary B cells from cord blood blood
7 chr21:16500200-16501800 Enhancers Primary B cells from peripheral blood blood
8 chr21:16500400-16505800 Weak transcription Small Intestine intestine
9 chr21:16500600-16502000 Weak transcription Primary hematopoietic stem cells blood
10 chr21:16500600-16510800 Weak transcription Psoas Muscle Psoas
11 chr21:16500800-16502200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr21:16500800-16505800 Weak transcription Duodenum Mucosa Duodenum
13 chr21:16501200-16506000 Weak transcription Monocytes-CD14+_RO01746 blood

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