Variant report

Variant rs537388836
Chromosome Location chr18:29371724-29371725
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29363200-29375600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr18:29367800-29372200 Weak transcription Fetal Intestine Large intestine
3 chr18:29368400-29372200 Weak transcription Fetal Intestine Small intestine
4 chr18:29369600-29373600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr18:29369600-29375000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr18:29369600-29377200 Weak transcription H9 Cell Line embryonic stem cell
7 chr18:29370400-29372800 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr18:29371000-29372600 Enhancers Primary monocytes fromperipheralblood blood
9 chr18:29371000-29373000 Enhancers HepG2 liver
10 chr18:29371000-29373800 Enhancers Monocytes-CD14+_RO01746 blood
11 chr18:29371200-29373600 Enhancers Liver Liver
12 chr18:29371400-29372000 Enhancers Primary hematopoietic stem cells blood
13 chr18:29371400-29372200 Enhancers Primary B cells from peripheral blood blood
14 chr18:29371400-29372200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr18:29371400-29372400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
16 chr18:29371400-29372600 Enhancers Primary Natural Killer cells fromperipheralblood blood
17 chr18:29371600-29372000 Enhancers GM12878-XiMat blood

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