Variant report

Variant rs73577464
Chromosome Location chr8:49773883-49773884
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49765400-49776600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr8:49768200-49775200 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr8:49771800-49776000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
4 chr8:49772800-49775800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr8:49772800-49777000 Weak transcription H9 Cell Line embryonic stem cell
6 chr8:49773000-49774800 Weak transcription Fetal Kidney kidney
7 chr8:49773000-49775600 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr8:49773200-49775800 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr8:49773200-49779200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
10 chr8:49773400-49774600 Weak transcription Fetal Lung lung
11 chr8:49773600-49774400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr8:49773600-49775400 Weak transcription Right Atrium heart
13 chr8:49773600-49777400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
14 chr8:49773800-49774200 Weak transcription Fetal Brain Male brain

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