Variant report

Variant rs17728008
Chromosome Location chr12:7985460-7985461
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:7953600-7987400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr12:7979600-7986600 Weak transcription Placenta Amnion Placenta Amnion
3 chr12:7983200-7986600 Weak transcription Fetal Adrenal Gland Adrenal Gland
4 chr12:7984800-7987200 Enhancers Primary neutrophils fromperipheralblood blood
5 chr12:7984800-7988800 Enhancers HepG2 liver
6 chr12:7985000-7985600 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr12:7985000-7985600 Enhancers Primary B cells from cord blood blood
8 chr12:7985000-7985800 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr12:7985000-7988000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr12:7985200-7985600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr12:7985200-7985800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
12 chr12:7985200-7987600 Weak transcription HUES6 Cell Line embryonic stem cell
13 chr12:7985400-7986800 Weak transcription Monocytes-CD14+_RO01746 blood
14 chr12:7985400-7987000 Weak transcription Primary monocytes fromperipheralblood blood
15 chr12:7985400-7988600 Weak transcription HUES48 Cell Line embryonic stem cell
16 chr12:7985400-7996800 Weak transcription HUES64 Cell Line embryonic stem cell
17 chr12:7985400-7997600 Weak transcription iPS-18 Cell Line embryonic stem cell

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