Variant report

Variant rs7118842
Chromosome Location chr11:16102092-16102093
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16068800-16103800 Weak transcription Left Ventricle heart
2 chr11:16083200-16116000 Weak transcription Fetal Intestine Large intestine
3 chr11:16089400-16117400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:16093400-16103200 Weak transcription Fetal Intestine Small intestine
5 chr11:16097000-16115600 Weak transcription Psoas Muscle Psoas
6 chr11:16097200-16103800 Weak transcription Duodenum Mucosa Duodenum
7 chr11:16097200-16104400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr11:16098400-16104200 Weak transcription Liver Liver
9 chr11:16098600-16137000 Weak transcription Pancreas Pancrea
10 chr11:16099000-16103200 Weak transcription Fetal Lung lung
11 chr11:16099800-16102200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr11:16100000-16103400 Weak transcription Brain Germinal Matrix brain
13 chr11:16100400-16107800 Weak transcription Esophagus oesophagus
14 chr11:16101800-16105000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
15 chr11:16101800-16109600 Enhancers Cortex derived primary cultured neurospheres brain
16 chr11:16102000-16102800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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