Variant report

Variant rs4851187
Chromosome Location chr2:99745860-99745861
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:99739200-99746000 Weak transcription Primary B cells from cord blood blood
2 chr2:99741800-99746800 Weak transcription Placenta Amnion Placenta Amnion
3 chr2:99742800-99757200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr2:99743200-99746000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr2:99743200-99757000 Weak transcription Small Intestine intestine
6 chr2:99743400-99756400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:99743400-99756600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:99743400-99756800 Weak transcription Brain Cingulate Gyrus brain

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