Variant report

Variant rs17155389
Chromosome Location chr10:44670020-44670021
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:44656600-44673200 Weak transcription Right Atrium heart
2 chr10:44667000-44670600 Enhancers Breast Myoepithelial Primary Cells Breast
3 chr10:44667400-44671400 Weak transcription Right Ventricle heart
4 chr10:44667400-44675800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chr10:44668600-44679600 Weak transcription Left Ventricle heart
6 chr10:44669200-44670200 Weak transcription Stomach Smooth Muscle stomach
7 chr10:44669200-44671800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr10:44669400-44671600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr10:44669400-44671800 Weak transcription Fetal Lung lung
10 chr10:44669400-44672600 Weak transcription NHDF-Ad bronchial
11 chr10:44669600-44670200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr10:44669600-44671000 Weak transcription Fetal Kidney kidney
13 chr10:44669600-44671600 Weak transcription HepG2 liver
14 chr10:44669600-44674600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr10:44669600-44674800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr10:44670000-44670400 Enhancers Pancreas Pancrea
17 chr10:44670000-44671800 Weak transcription Fetal Heart heart

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