Variant report

Variant rs11696281
Chromosome Location chr20:24914488-24914489
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:24901400-24915200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr20:24911000-24914600 Enhancers Primary T cells fromperipheralblood blood
3 chr20:24911000-24914600 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr20:24911000-24914600 Enhancers Primary Natural Killer cells fromperipheralblood blood
5 chr20:24911000-24915200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr20:24911400-24915800 Enhancers Thymus Thymus
7 chr20:24911800-24914600 Enhancers Placenta Placenta
8 chr20:24912000-24914600 Enhancers Dnd41 blood
9 chr20:24912200-24915000 Weak transcription Esophagus oesophagus
10 chr20:24913200-24915400 Enhancers Pancreas Pancrea
11 chr20:24913200-24916400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr20:24913400-24915400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr20:24913800-24915600 Enhancers Fetal Intestine Large intestine
14 chr20:24914000-24914800 Bivalent Enhancer Fetal Muscle Trunk muscle
15 chr20:24914000-24915600 Enhancers Fetal Intestine Small intestine
16 chr20:24914000-24915800 Enhancers Duodenum Mucosa Duodenum
17 chr20:24914000-24916000 Enhancers Fetal Thymus thymus
18 chr20:24914200-24914600 Weak transcription Gastric stomach
19 chr20:24914400-24915000 Weak transcription Spleen Spleen

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