Variant report

Variant rs11183893
Chromosome Location chr12:47740314-47740315
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:47723200-47742200 Weak transcription Primary T cells from cord blood blood
2 chr12:47737400-47748400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr12:47737600-47741600 Enhancers Liver Liver
4 chr12:47739800-47740400 Enhancers Fetal Intestine Large intestine
5 chr12:47739800-47740400 Enhancers Fetal Intestine Small intestine
6 chr12:47740000-47740600 Enhancers Pancreatic Islets Pancreatic Islet
7 chr12:47740000-47741000 Enhancers Stomach Mucosa stomach
8 chr12:47740000-47741000 Enhancers A549 lung
9 chr12:47740000-47741200 Enhancers HepG2 liver
10 chr12:47740200-47740800 Enhancers Primary monocytes fromperipheralblood blood
11 chr12:47740200-47740800 Enhancers Primary T helper naive cells fromperipheralblood blood
12 chr12:47740200-47740800 Enhancers Osteobl bone
13 chr12:47740200-47741000 Enhancers Monocytes-CD14+_RO01746 blood
14 chr12:47740200-47742400 Enhancers Primary T helper cells PMA-I stimulated --

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