Variant report

Variant rs35389351
Chromosome Location chr6:53639054-53639055
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:53632000-53639600 Weak transcription Placenta Amnion Placenta Amnion
2 chr6:53636400-53652800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:53637600-53656000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr6:53638800-53639400 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr6:53638800-53639400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
6 chr6:53638800-53639400 ZNF genes & repeats Fetal Intestine Small intestine

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