Variant report

Variant rs61958138
Chromosome Location chr13:53182367-53182368
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:53173800-53182400 Weak transcription Fetal Heart heart
2 chr13:53175000-53191000 Weak transcription Fetal Stomach stomach
3 chr13:53175200-53183200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr13:53175200-53183200 Weak transcription Stomach Smooth Muscle stomach
5 chr13:53177600-53182400 Weak transcription HepG2 liver
6 chr13:53180000-53182600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
7 chr13:53181200-53190000 Weak transcription Monocytes-CD14+_RO01746 blood
8 chr13:53181800-53183000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
9 chr13:53182200-53182400 Enhancers Breast Myoepithelial Primary Cells Breast
10 chr13:53182200-53183200 Weak transcription iPS-15b Cell Line embryonic stem cell
11 chr13:53182200-53183800 Enhancers HUVEC blood vessel

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