Variant report

Variant rs10899308
Chromosome Location chr11:76619742-76619743
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:76597000-76631000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr11:76608800-76622600 Weak transcription Left Ventricle heart
3 chr11:76613600-76631200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr11:76613800-76622200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
5 chr11:76613800-76622600 Weak transcription H9 Cell Line embryonic stem cell
6 chr11:76615000-76620200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr11:76615600-76622200 Weak transcription Small Intestine intestine
8 chr11:76615600-76631200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr11:76617600-76622400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr11:76617800-76621600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr11:76617800-76622000 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr11:76617800-76630000 Weak transcription Primary monocytes fromperipheralblood blood
13 chr11:76617800-76630000 Weak transcription Cortex derived primary cultured neurospheres brain
14 chr11:76618200-76637600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr11:76618600-76629800 Weak transcription A549 lung
16 chr11:76618600-76630000 Weak transcription Monocytes-CD14+_RO01746 blood

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