Variant report

Variant rs60349325
Chromosome Location chr11:75891850-75891851
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:75883600-75897000 Weak transcription Fetal Intestine Small intestine
2 chr11:75887600-75892000 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr11:75887800-75896400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr11:75888200-75895200 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr11:75888800-75894800 Weak transcription Fetal Lung lung
6 chr11:75890600-75897000 Weak transcription Gastric stomach
7 chr11:75890800-75895200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr11:75891000-75896000 Weak transcription Placenta Amnion Placenta Amnion
9 chr11:75891200-75892000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr11:75891200-75892400 Enhancers Fetal Muscle Trunk muscle
11 chr11:75891400-75892000 Enhancers HepG2 liver
12 chr11:75891400-75892200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr11:75891800-75892000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
14 chr11:75891800-75893400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
15 chr11:75891800-75893600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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