Variant report

Variant rs77934546
Chromosome Location chr2:180068349-180068350
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180066800-180068400 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:180066800-180068800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
3 chr2:180067000-180068400 ZNF genes & repeats Primary hematopoietic stem cells blood
4 chr2:180067000-180068600 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
5 chr2:180067000-180069200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr2:180067200-180068800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr2:180067400-180068400 ZNF genes & repeats Fetal Intestine Large intestine
8 chr2:180067400-180068600 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung
9 chr2:180067600-180068600 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr2:180067600-180097600 Weak transcription Primary B cells from cord blood blood
11 chr2:180067600-180104600 Weak transcription Fetal Kidney kidney
12 chr2:180067800-180068800 ZNF genes & repeats Fetal Intestine Small intestine
13 chr2:180068000-180071000 Weak transcription Brain Inferior Temporal Lobe brain
14 chr2:180068000-180071400 Weak transcription Pancreatic Islets Pancreatic Islet
15 chr2:180068000-180103800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr2:180068200-180068400 Strong transcription Fetal Stomach stomach

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