Variant report

Variant rs7111234
Chromosome Location chr11:75891033-75891034
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr11:75890600-75891400 Flanking Active TSS HepG2 liver
7 chr11:75890600-75897000 Weak transcription Gastric stomach
8 chr11:75890800-75891800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
9 chr11:75890800-75895200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr11:75891000-75891400 Genic enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr11:75891000-75891800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr11:75891000-75896000 Weak transcription Placenta Amnion Placenta Amnion

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