Variant report

Variant rs57588070
Chromosome Location chr11:77299451-77299452
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:77280800-77299600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
2 chr11:77287800-77299600 Weak transcription Ovary ovary
3 chr11:77293000-77299800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr11:77294800-77300000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
5 chr11:77296000-77299800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr11:77298400-77299600 Weak transcription Duodenum Mucosa Duodenum
7 chr11:77298600-77299600 Weak transcription Fetal Intestine Small intestine
8 chr11:77299200-77299600 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr11:77299400-77299600 Enhancers Colonic Mucosa Colon
10 chr11:77299400-77299600 Enhancers Fetal Adrenal Gland Adrenal Gland
11 chr11:77299400-77299600 Enhancers Right Ventricle heart
12 chr11:77299400-77299800 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr11:77299400-77299800 Enhancers Primary T helper naive cells fromperipheralblood blood
14 chr11:77299400-77299800 Weak transcription Dnd41 blood
15 chr11:77299400-77299800 Enhancers Osteobl bone
16 chr11:77299400-77300000 Active TSS Hela-S3 cervix
17 chr11:77299400-77300200 Flanking Active TSS Placenta Placenta

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