Variant report

Variant rs11698426
Chromosome Location chr20:24914663-24914664
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr20:24911000-24915200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chr20:24911400-24915800 Enhancers Thymus Thymus
4 chr20:24912200-24915000 Weak transcription Esophagus oesophagus
5 chr20:24913200-24915400 Enhancers Pancreas Pancrea
6 chr20:24913200-24916400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr20:24913400-24915400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr20:24913800-24915600 Enhancers Fetal Intestine Large intestine
9 chr20:24914000-24914800 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr20:24914000-24915600 Enhancers Fetal Intestine Small intestine
11 chr20:24914000-24915800 Enhancers Duodenum Mucosa Duodenum
12 chr20:24914000-24916000 Enhancers Fetal Thymus thymus
13 chr20:24914400-24915000 Weak transcription Spleen Spleen
14 chr20:24914600-24915000 Enhancers Gastric stomach

Quick Search:


  
Input of quick search could be:

what's new

Quick links