Variant report

Variant rs1973616
Chromosome Location chr4:189326092-189326093
allele C/G/T
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 chr4:189322600-189326800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr4:189323400-189327000 Enhancers HMEC breast
5 chr4:189323400-189328200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
6 chr4:189323600-189326200 Transcr. at gene 5' and 3' Breast Myoepithelial Primary Cells Breast
7 chr4:189323800-189326400 Transcr. at gene 5' and 3' Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr4:189323800-189329000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr4:189325200-189326200 Flanking Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr4:189325200-189327600 Weak transcription Duodenum Smooth Muscle Duodenum
11 chr4:189325400-189326200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr4:189325400-189326200 Flanking Active TSS Osteobl bone
13 chr4:189325400-189327000 Enhancers NHDF-Ad bronchial
14 chr4:189325600-189326400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr4:189325800-189326200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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