Variant report

Variant rs4756678
Chromosome Location chr11:33430037-33430038
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:33413400-33466200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:33415600-33434000 Weak transcription Fetal Brain Female brain
3 chr11:33423800-33433000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:33423800-33433400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr11:33423800-33434000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr11:33424000-33432400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr11:33424000-33440200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
8 chr11:33428200-33431400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr11:33428400-33432000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr11:33429600-33433600 Weak transcription Pancreatic Islets Pancreatic Islet

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