Variant report

Variant rs6854641
Chromosome Location chr4:189324617-189324618
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr4:189322600-189325400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr4:189322600-189325800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr4:189322600-189326800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:189322800-189325400 Weak transcription NHDF-Ad bronchial
7 chr4:189323200-189325600 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr4:189323400-189327000 Enhancers HMEC breast
9 chr4:189323400-189328200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr4:189323600-189326200 Transcr. at gene 5' and 3' Breast Myoepithelial Primary Cells Breast
11 chr4:189323800-189326400 Transcr. at gene 5' and 3' Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr4:189323800-189329000 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr4:189324000-189325800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr4:189324200-189324800 Enhancers H1 Cell Line embryonic stem cell
15 chr4:189324200-189325200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr4:189324600-189324800 Genic enhancers Osteobl bone

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