Variant report

Variant rs7947622
Chromosome Location chr11:16090308-16090309
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16043000-16102000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr11:16068800-16103800 Weak transcription Left Ventricle heart
3 chr11:16074800-16092200 Weak transcription Fetal Intestine Small intestine
4 chr11:16075200-16092600 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr11:16083200-16116000 Weak transcription Fetal Intestine Large intestine
6 chr11:16083600-16096400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
7 chr11:16088200-16092200 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr11:16088200-16096600 Weak transcription Psoas Muscle Psoas
9 chr11:16088600-16099000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr11:16089400-16117400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:16089600-16094400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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