Variant report

Variant rs13110644
Chromosome Location chr4:101744246-101744247
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:101740000-101745600 Weak transcription Pancreatic Islets Pancreatic Islet
2 chr4:101741200-101744600 Weak transcription iPS-20b Cell Line embryonic stem cell
3 chr4:101743200-101745200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr4:101743600-101745000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr4:101743800-101745200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:101743800-101745400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr4:101743800-101745400 Enhancers NHEK skin
8 chr4:101744000-101744600 Enhancers A549 lung
9 chr4:101744000-101744600 Enhancers GM12878-XiMat blood
10 chr4:101744000-101744800 Enhancers Muscle Satellite Cultured Cells --
11 chr4:101744000-101745000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr4:101744000-101745000 Enhancers HSMM muscle
13 chr4:101744000-101745000 Enhancers NH-A brain
14 chr4:101744000-101746000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
15 chr4:101744200-101745000 Enhancers Placenta Amnion Placenta Amnion
16 chr4:101744200-101745200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
17 chr4:101744200-101745200 Enhancers Fetal Adrenal Gland Adrenal Gland
18 chr4:101744200-101745200 Enhancers HMEC breast

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