Variant report

Variant rs73777468
Chromosome Location chr6:140499960-140499961
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:140496200-140501200 Weak transcription Placenta Placenta
2 chr6:140497000-140500000 Weak transcription HMEC breast
3 chr6:140497000-140516400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:140498200-140504400 Weak transcription K562 blood
5 chr6:140498600-140501400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr6:140499000-140501200 Enhancers NHDF-Ad bronchial
7 chr6:140499200-140500000 Enhancers Ovary ovary
8 chr6:140499200-140500000 Enhancers NHLF lung
9 chr6:140499200-140500800 Enhancers Osteobl bone
10 chr6:140499200-140501000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
11 chr6:140499200-140501400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr6:140499400-140500000 Enhancers Colon Smooth Muscle Colon
13 chr6:140499400-140500600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
14 chr6:140499400-140500800 Enhancers Muscle Satellite Cultured Cells --
15 chr6:140499600-140500600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
16 chr6:140499800-140500000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr6:140499800-140500200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
18 chr6:140499800-140500200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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