Variant report

Variant rs12997546
Chromosome Location chr2:180407753-180407754
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180403200-180408000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr2:180403800-180408000 Weak transcription Osteobl bone
3 chr2:180403800-180408600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:180403800-180408600 Weak transcription Fetal Kidney kidney
5 chr2:180403800-180409800 Weak transcription Skeletal Muscle Male skeletal muscle
6 chr2:180404000-180408000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr2:180404000-180410000 Strong transcription Liver Liver
8 chr2:180404200-180409800 Weak transcription Gastric stomach
9 chr2:180405400-180410600 Enhancers HepG2 liver
10 chr2:180405800-180408000 Weak transcription Fetal Adrenal Gland Adrenal Gland
11 chr2:180406800-180407800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
12 chr2:180407000-180411400 Weak transcription Right Atrium heart
13 chr2:180407400-180408800 Enhancers Muscle Satellite Cultured Cells --
14 chr2:180407600-180408400 Genic enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell

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