Variant report

Variant rs73257114
Chromosome Location chr6:167688894-167688895
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr6:167683000-167690200 Weak transcription Liver Liver
3 chr6:167685000-167691800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr6:167685800-167691600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr6:167687000-167690400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:167688000-167689200 Enhancers Placenta Amnion Placenta Amnion
7 chr6:167688000-167689400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr6:167688000-167689400 Enhancers Esophagus oesophagus
9 chr6:167688000-167691600 Weak transcription H9 Cell Line embryonic stem cell
10 chr6:167688400-167689200 Enhancers Lung lung
11 chr6:167688400-167690000 Weak transcription Fetal Intestine Large intestine
12 chr6:167688600-167689000 Enhancers Gastric stomach
13 chr6:167688600-167692600 Weak transcription Fetal Intestine Small intestine
14 chr6:167688800-167689400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:167688800-167689400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
16 chr6:167688800-167690200 Weak transcription HepG2 liver

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