Variant report

Variant rs71482998
Chromosome Location chr11:16127188-16127189
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16098600-16137000 Weak transcription Pancreas Pancrea
2 chr11:16119600-16130200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr11:16120800-16130800 Weak transcription Esophagus oesophagus
4 chr11:16121600-16135400 Weak transcription Fetal Intestine Large intestine
5 chr11:16121800-16136800 Weak transcription Small Intestine intestine
6 chr11:16122400-16132400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:16126800-16128000 ZNF genes & repeats Cortex derived primary cultured neurospheres brain
8 chr11:16126800-16128600 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
9 chr11:16127000-16127400 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr11:16127000-16127400 ZNF genes & repeats Liver Liver

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