Variant report

Variant rs4936507
Chromosome Location chr11:119934563-119934564
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:119922600-119936000 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr11:119931800-119935200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr11:119932000-119935000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
4 chr11:119932400-119935400 Enhancers Fetal Brain Male brain
5 chr11:119932600-119934800 Enhancers Brain Cingulate Gyrus brain
6 chr11:119932600-119935200 Enhancers Brain Angular Gyrus brain
7 chr11:119933400-119935400 Enhancers Fetal Brain Female brain
8 chr11:119933600-119934600 Weak transcription Brain Substantia Nigra brain
9 chr11:119933600-119934800 Weak transcription Esophagus oesophagus
10 chr11:119933600-119934800 Weak transcription Fetal Lung lung
11 chr11:119933600-119938000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr11:119933800-119936800 Weak transcription Brain Inferior Temporal Lobe brain
13 chr11:119933800-119938400 Weak transcription Fetal Kidney kidney
14 chr11:119933800-119939000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr11:119934200-119934800 Enhancers Brain Hippocampus Middle brain
16 chr11:119934200-119939000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
17 chr11:119934400-119934800 Enhancers Brain Dorsolateral Prefrontal Cortex brain
18 chr11:119934400-119934800 Bivalent Enhancer Fetal Stomach stomach

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