Variant report

Variant rs16843626
Chromosome Location chr2:210598862-210598863
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210552800-210599400 Weak transcription Pancreas Pancrea
2 chr2:210555600-210600200 Weak transcription Left Ventricle heart
3 chr2:210581000-210600600 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr2:210585000-210600000 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:210586600-210599600 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:210586800-210599800 Strong transcription Cortex derived primary cultured neurospheres brain
7 chr2:210588800-210599400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:210589600-210600800 Weak transcription Brain Angular Gyrus brain
9 chr2:210591800-210599200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:210592000-210599000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr2:210595200-210601400 Weak transcription Aorta Aorta
12 chr2:210595800-210602200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr2:210598200-210599400 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr2:210598200-210600200 Weak transcription Brain Germinal Matrix brain
15 chr2:210598400-210603000 Weak transcription Fetal Brain Female brain

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