Variant report

Variant rs4242484
Chromosome Location chr8:49089947-49089948
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49084400-49090600 Enhancers Fetal Stomach stomach
2 chr8:49085200-49098400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr8:49087200-49091400 Weak transcription Gastric stomach
4 chr8:49088000-49090200 Weak transcription Fetal Kidney kidney
5 chr8:49088800-49090000 Weak transcription Colonic Mucosa Colon
6 chr8:49088800-49090200 Weak transcription Fetal Lung lung
7 chr8:49089200-49090200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr8:49089200-49091800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr8:49089600-49094000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr8:49089800-49090000 Enhancers Fetal Intestine Small intestine
11 chr8:49089800-49091400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell

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