Variant report

Variant rs143003770
Chromosome Location chr6:121895799-121895800
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:121892400-121895800 Enhancers Fetal Intestine Large intestine
2 chr6:121892800-121895800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr6:121892800-121896000 Weak transcription H9 Cell Line embryonic stem cell
4 chr6:121893600-121895800 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr6:121894200-121895800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr6:121894400-121895800 Enhancers HUVEC blood vessel
7 chr6:121894600-121895800 Enhancers Ovary ovary
8 chr6:121894800-121895800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
9 chr6:121895000-121895800 Enhancers Left Ventricle heart
10 chr6:121895200-121895800 Enhancers Brain Substantia Nigra brain
11 chr6:121895200-121895800 Enhancers Right Ventricle heart
12 chr6:121895200-121896000 Enhancers Primary monocytes fromperipheralblood blood
13 chr6:121895400-121895800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr6:121895400-121899800 Weak transcription Small Intestine intestine
15 chr6:121895400-121905400 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr6:121895600-121895800 Enhancers Monocytes-CD14+_RO01746 blood

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