Variant report

Variant rs11895749
Chromosome Location chr2:99746290-99746291
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:6 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:99741800-99746800 Weak transcription Placenta Amnion Placenta Amnion
2 chr2:99742800-99757200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr2:99743200-99757000 Weak transcription Small Intestine intestine
4 chr2:99743400-99756400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:99743400-99756600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr2:99743400-99756800 Weak transcription Brain Cingulate Gyrus brain

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