Variant report

Variant rs55968717
Chromosome Location chr6:167690983-167690984
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167685000-167691800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr6:167685800-167691600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr6:167688000-167691600 Weak transcription H9 Cell Line embryonic stem cell
4 chr6:167688600-167692600 Weak transcription Fetal Intestine Small intestine
5 chr6:167689000-167694800 Weak transcription Gastric stomach
6 chr6:167689200-167702400 Weak transcription Placenta Amnion Placenta Amnion
7 chr6:167690200-167691400 Enhancers Liver Liver
8 chr6:167690200-167691600 Enhancers HepG2 liver
9 chr6:167690600-167692000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr6:167690800-167695000 Enhancers HUES6 Cell Line embryonic stem cell
11 chr6:167690800-167695200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr6:167690800-167698600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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