Variant report

Variant rs2171708
Chromosome Location chr8:111846636-111846637
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:111840400-111847200 Weak transcription Fetal Lung lung
2 chr8:111842200-111847000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
3 chr8:111842200-111847200 Weak transcription H9 Cell Line embryonic stem cell
4 chr8:111842600-111847200 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr8:111842600-111848200 Weak transcription H1 Cell Line embryonic stem cell
6 chr8:111842800-111846800 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr8:111842800-111847200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr8:111844400-111847200 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr8:111844600-111847400 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr8:111845200-111847000 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr8:111845200-111847000 Weak transcription HUES6 Cell Line embryonic stem cell
12 chr8:111846200-111847000 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr8:111846200-111847200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr8:111846600-111847600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
15 chr8:111846600-111849400 Enhancers HUES64 Cell Line embryonic stem cell

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