Variant report

Variant rs188896962
Chromosome Location chr18:29007590-29007591
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:8 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr18:29004400-29008200 Weak transcription Stomach Mucosa stomach
2 chr18:29004400-29009200 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr18:29006600-29010600 Enhancers Placenta Amnion Placenta Amnion
4 chr18:29007200-29007800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr18:29007200-29008800 Weak transcription HMEC breast
6 chr18:29007200-29010800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr18:29007400-29008400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr18:29007400-29010800 Enhancers NHEK skin

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