Variant report

Variant rs2697188
Chromosome Location chr7:121073357-121073358
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:121069000-121073400 Weak transcription Placenta Placenta
2 chr7:121069200-121077600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr7:121069400-121074400 Weak transcription Placenta Amnion Placenta Amnion
4 chr7:121069800-121078000 Weak transcription Fetal Kidney kidney
5 chr7:121072200-121077600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr7:121072400-121074000 Weak transcription Fetal Intestine Large intestine
7 chr7:121072400-121074200 Weak transcription Fetal Intestine Small intestine
8 chr7:121073000-121074400 Flanking Active TSS GM12878-XiMat blood

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