Variant report

Variant rs10838635
Chromosome Location chr11:46945227-46945228
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr11:46941400-46946400 Weak transcription Hela-S3 cervix
4 chr11:46941800-46945400 Weak transcription Stomach Mucosa stomach
5 chr11:46943000-46946800 Weak transcription Colon Smooth Muscle Colon
6 chr11:46943000-46951800 Weak transcription NHEK skin
7 chr11:46944600-46945600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr11:46944600-46946000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr11:46944800-46958200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr11:46945200-46945400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr11:46945200-46945400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr11:46945200-46945400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr11:46945200-46945400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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