Variant report

Variant rs11833714
Chromosome Location chr12:103953723-103953724
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:103950200-103955600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
2 chr12:103951200-103956600 Enhancers Placenta Placenta
3 chr12:103951600-103954000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
4 chr12:103951600-103954600 Weak transcription Fetal Muscle Leg muscle
5 chr12:103952400-103956000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr12:103952600-103954000 Enhancers A549 lung
7 chr12:103952800-103954200 Enhancers NHEK skin
8 chr12:103952800-103956800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr12:103952800-103958200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr12:103953200-103954000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr12:103953200-103954000 Weak transcription Fetal Intestine Large intestine
12 chr12:103953200-103956400 Enhancers HMEC breast
13 chr12:103953400-103953800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr12:103953400-103955600 Enhancers NHDF-Ad bronchial
15 chr12:103953600-103955400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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