Variant report

Variant rs1836467
Chromosome Location chr10:45774725-45774726
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:45774400-45774800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr10:45774400-45774800 Enhancers Gastric stomach
3 chr10:45774400-45775000 Enhancers Fetal Intestine Small intestine
4 chr10:45774400-45775000 Enhancers Pancreas Pancrea
5 chr10:45774400-45775000 Flanking Active TSS K562 blood
6 chr10:45774400-45776000 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr10:45774400-45776000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr10:45774400-45776600 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr10:45774400-45777200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr10:45774600-45774800 Enhancers Left Ventricle heart
11 chr10:45774600-45774800 Enhancers Right Atrium heart
12 chr10:45774600-45775800 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr10:45774600-45776200 Enhancers Fetal Intestine Large intestine
14 chr10:45774600-45778400 Enhancers Stomach Mucosa stomach

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