Variant report

Variant rs11833672
Chromosome Location chr12:103953392-103953393
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:103948200-103953400 Weak transcription NHDF-Ad bronchial
2 chr12:103950200-103955600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr12:103951200-103956600 Enhancers Placenta Placenta
4 chr12:103951600-103953600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr12:103951600-103954000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr12:103951600-103954600 Weak transcription Fetal Muscle Leg muscle
7 chr12:103952400-103956000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
8 chr12:103952600-103954000 Enhancers A549 lung
9 chr12:103952800-103953400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr12:103952800-103954200 Enhancers NHEK skin
11 chr12:103952800-103956800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr12:103952800-103958200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr12:103953200-103954000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
14 chr12:103953200-103954000 Weak transcription Fetal Intestine Large intestine
15 chr12:103953200-103956400 Enhancers HMEC breast

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