Variant report

Variant rs35110659
Chromosome Location chr12:7992820-7992821
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:7985400-7996800 Weak transcription HUES64 Cell Line embryonic stem cell
2 chr12:7985400-7997600 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr12:7987200-7994200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
4 chr12:7987800-7994800 Weak transcription Fetal Adrenal Gland Adrenal Gland
5 chr12:7988000-7995200 Enhancers Primary neutrophils fromperipheralblood blood
6 chr12:7988800-7999800 Weak transcription HepG2 liver
7 chr12:7991200-7994200 Weak transcription Primary B cells from cord blood blood
8 chr12:7991400-7994600 Weak transcription Primary monocytes fromperipheralblood blood
9 chr12:7991400-7994800 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr12:7992200-7993000 Enhancers Fetal Brain Male brain
11 chr12:7992600-7994800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr12:7992600-7997200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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