Variant report

Variant rs369134507
Chromosome Location chr1:175388855-175388856
allele -/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:175370000-175390200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:175385000-175390200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr1:175388800-175389000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr1:175388800-175389000 Enhancers Fetal Intestine Large intestine
5 chr1:175388800-175389800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:175388800-175393000 Enhancers Fetal Intestine Small intestine

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