Variant report

Variant rs59645198
Chromosome Location chr4:189328715-189328716
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:189320800-189329000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr4:189322400-189329000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr4:189323800-189329000 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr4:189327000-189329000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr4:189327000-189329000 Weak transcription HMEC breast
6 chr4:189327000-189329200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr4:189327800-189329200 Genic enhancers Breast Myoepithelial Primary Cells Breast
8 chr4:189328000-189329000 Genic enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr4:189328000-189331800 Enhancers NHDF-Ad bronchial
10 chr4:189328400-189328800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
11 chr4:189328400-189329000 Genic enhancers Osteobl bone
12 chr4:189328400-189329800 Enhancers Fetal Intestine Large intestine
13 chr4:189328400-189330200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr4:189328400-189331800 Enhancers Fetal Intestine Small intestine
15 chr4:189328600-189329400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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