Variant report

Variant rs10188807
Chromosome Location chr2:187177409-187177410
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187171400-187179400 Weak transcription Brain Substantia Nigra brain
2 chr2:187173200-187192200 Weak transcription Placenta Amnion Placenta Amnion
3 chr2:187173400-187177600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr2:187173600-187190000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:187176000-187178000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr2:187176200-187177600 Weak transcription Fetal Intestine Small intestine
7 chr2:187176600-187177600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr2:187177000-187179200 Weak transcription Ovary ovary

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