Variant report

Variant rs143361773
Chromosome Location chr2:180067451-180067452
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180032200-180067600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr2:180065600-180068200 Weak transcription Fetal Stomach stomach
3 chr2:180066800-180067600 ZNF genes & repeats Fetal Kidney kidney
4 chr2:180066800-180067800 ZNF genes & repeats HepG2 liver
5 chr2:180066800-180068400 ZNF genes & repeats Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:180066800-180068800 ZNF genes & repeats iPS-20b Cell Line embryonic stem cell
7 chr2:180067000-180068400 ZNF genes & repeats Primary hematopoietic stem cells blood
8 chr2:180067000-180068600 ZNF genes & repeats Monocytes-CD14+_RO01746 blood
9 chr2:180067000-180069200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr2:180067200-180068000 ZNF genes & repeats Pancreatic Islets Pancreatic Islet
11 chr2:180067200-180068200 ZNF genes & repeats Fetal Muscle Trunk muscle
12 chr2:180067200-180068800 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr2:180067400-180068000 ZNF genes & repeats Brain Inferior Temporal Lobe brain
14 chr2:180067400-180068400 ZNF genes & repeats Fetal Intestine Large intestine
15 chr2:180067400-180068600 ZNF genes & repeats IMR90 fetal lung fibroblasts Cell Line lung

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