Variant report

Variant rs10861038
Chromosome Location chr12:103953057-103953058
allele A/C
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 chr12:103952200-103953200 Weak transcription HMEC breast
8 chr12:103952400-103956000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr12:103952600-103953200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr12:103952600-103954000 Enhancers A549 lung
11 chr12:103952800-103953200 Enhancers Fetal Intestine Large intestine
12 chr12:103952800-103953400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr12:103952800-103954200 Enhancers NHEK skin
14 chr12:103952800-103956800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr12:103952800-103958200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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