Variant report

Variant rs59555466
Chromosome Location chr7:41026640-41026641
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41011800-41042000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr7:41019200-41036200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr7:41020800-41034200 Weak transcription Aorta Aorta
4 chr7:41024200-41028200 Enhancers Hela-S3 cervix
5 chr7:41024400-41027400 Enhancers Pancreatic Islets Pancreatic Islet
6 chr7:41024800-41026800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr7:41024800-41027000 Enhancers Osteobl bone
8 chr7:41025000-41026800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr7:41025000-41026800 Enhancers NHLF lung
10 chr7:41025000-41027000 Enhancers Muscle Satellite Cultured Cells --
11 chr7:41025400-41027000 Enhancers NHDF-Ad bronchial
12 chr7:41026400-41026800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
13 chr7:41026400-41027600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr7:41026600-41029800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
15 chr7:41026600-41030000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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