Variant report

Variant rs60098363
Chromosome Location chr7:17700717-17700718
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:17683800-17701800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr7:17692000-17701800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr7:17695800-17701600 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr7:17698400-17701800 Weak transcription Esophagus oesophagus
5 chr7:17698800-17701800 Enhancers NHDF-Ad bronchial
6 chr7:17699000-17703800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr7:17699600-17701800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr7:17699600-17703400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr7:17699600-17703600 Enhancers HMEC breast
10 chr7:17699800-17701800 Enhancers NHEK skin
11 chr7:17699800-17703600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:17699800-17703800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr7:17700000-17703800 Enhancers Breast Myoepithelial Primary Cells Breast
14 chr7:17700200-17701200 Weak transcription Muscle Satellite Cultured Cells --
15 chr7:17700600-17701000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
16 chr7:17700600-17701000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
17 chr7:17700600-17701000 Weak transcription Osteobl bone
18 chr7:17700600-17701600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin

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