Variant report

Variant rs10138952
Chromosome Location chr14:67536019-67536020
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67511600-67538000 Weak transcription Stomach Smooth Muscle stomach
2 chr14:67511600-67544600 Weak transcription Brain Hippocampus Middle brain
3 chr14:67511600-67544800 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
4 chr14:67511600-67556200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr14:67517800-67544400 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr14:67518000-67544800 Weak transcription Fetal Stomach stomach
7 chr14:67524000-67544600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr14:67527600-67551200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
9 chr14:67527800-67537800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
10 chr14:67529200-67549000 Weak transcription Adipose Nuclei Adipose
11 chr14:67529400-67542400 Weak transcription Liver Liver
12 chr14:67529400-67544600 Weak transcription Brain Inferior Temporal Lobe brain
13 chr14:67534600-67536200 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
14 chr14:67534800-67576400 Weak transcription Pancreas Pancrea
15 chr14:67535200-67536800 Enhancers Fetal Heart heart
16 chr14:67535400-67536200 Enhancers Fetal Adrenal Gland Adrenal Gland

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