Variant report

Variant rs1854852
Chromosome Location chr6:167687856-167687857
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167681800-167689000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:167682800-167688000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr6:167682800-167688400 Enhancers Fetal Intestine Large intestine
4 chr6:167682800-167688600 Enhancers Fetal Intestine Small intestine
5 chr6:167683000-167688000 Weak transcription Placenta Amnion Placenta Amnion
6 chr6:167683000-167688800 Enhancers HepG2 liver
7 chr6:167683000-167690200 Weak transcription Liver Liver
8 chr6:167685000-167691800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
9 chr6:167685600-167688000 Weak transcription Esophagus oesophagus
10 chr6:167685800-167691600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr6:167687000-167688600 Weak transcription Gastric stomach
12 chr6:167687000-167690400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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