Variant report

Variant rs10270768
Chromosome Location chr7:121074593-121074594
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:121069200-121077600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr7:121069800-121078000 Weak transcription Fetal Kidney kidney
3 chr7:121072200-121077600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr7:121073800-121076800 Weak transcription Primary B cells from peripheral blood blood
5 chr7:121074000-121074600 Enhancers Fetal Intestine Large intestine
6 chr7:121074000-121074600 Enhancers Placenta Placenta
7 chr7:121074200-121074600 Enhancers Fetal Intestine Small intestine
8 chr7:121074400-121074600 Enhancers GM12878-XiMat blood
9 chr7:121074400-121077400 Enhancers Placenta Amnion Placenta Amnion
10 chr7:121074400-121078000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr7:121074400-121080800 Weak transcription Pancreas Pancrea

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