Variant report

Variant rs434598
Chromosome Location chr17:43725762-43725763
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:43708800-43726200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr17:43714000-43726200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr17:43714200-43727800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr17:43715000-43725800 Weak transcription H1 Cell Line embryonic stem cell
5 chr17:43715000-43727000 Weak transcription Skeletal Muscle Female skeletal muscle
6 chr17:43715200-43726400 Weak transcription HUES6 Cell Line embryonic stem cell
7 chr17:43715200-43726400 Weak transcription iPS-15b Cell Line embryonic stem cell
8 chr17:43715200-43727200 Weak transcription Spleen Spleen
9 chr17:43716400-43736600 Weak transcription Right Atrium heart
10 chr17:43717200-43728000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
11 chr17:43718000-43726000 Weak transcription Breast Myoepithelial Primary Cells Breast
12 chr17:43723200-43728200 Weak transcription Fetal Brain Female brain
13 chr17:43724400-43729800 Weak transcription Brain Inferior Temporal Lobe brain
14 chr17:43725000-43728200 Enhancers Fetal Brain Male brain
15 chr17:43725400-43727200 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr17:43725600-43726200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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