Variant report

Variant rs10144919
Chromosome Location chr14:67249619-67249620
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:67225400-67256400 Weak transcription Pancreas Pancrea
2 chr14:67237600-67258800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr14:67238200-67256400 Weak transcription Liver Liver
4 chr14:67240000-67254800 Weak transcription Fetal Intestine Small intestine
5 chr14:67242600-67256200 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr14:67247400-67249800 Weak transcription Left Ventricle heart
7 chr14:67248400-67259000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr14:67248800-67251400 Weak transcription Fetal Lung lung
9 chr14:67248800-67251800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
10 chr14:67249000-67250200 Weak transcription Duodenum Mucosa Duodenum
11 chr14:67249600-67250200 Enhancers HepG2 liver
12 chr14:67249600-67250600 ZNF genes & repeats H9 Derived Neuron Cultured Cells ES cell derived

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