Variant report

Variant rs11039028
Chromosome Location chr11:46944196-46944197
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:46940600-46949600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr11:46940600-46951400 Weak transcription Placenta Amnion Placenta Amnion
3 chr11:46941200-46945200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr11:46941400-46946400 Weak transcription Hela-S3 cervix
5 chr11:46941800-46945400 Weak transcription Stomach Mucosa stomach
6 chr11:46942600-46945200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:46942800-46944400 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr11:46943000-46945200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr11:46943000-46946800 Weak transcription Colon Smooth Muscle Colon
10 chr11:46943000-46951800 Weak transcription NHEK skin
11 chr11:46943200-46944400 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr11:46943400-46944600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr11:46943400-46945200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr11:46943600-46944600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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