Variant report

Variant rs6986825
Chromosome Location chr8:49059396-49059397
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:49051800-49065800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr8:49054800-49059400 Weak transcription Muscle Satellite Cultured Cells --
3 chr8:49056200-49066000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr8:49058000-49064800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr8:49058200-49059800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr8:49058200-49060800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr8:49058600-49060000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr8:49058600-49060600 Enhancers Fetal Muscle Leg muscle
9 chr8:49058600-49060800 Enhancers Fetal Muscle Trunk muscle
10 chr8:49058800-49060600 Enhancers Fetal Stomach stomach
11 chr8:49059200-49059600 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
12 chr8:49059200-49059800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr8:49059200-49060000 Enhancers Aorta Aorta
14 chr8:49059200-49060000 Enhancers Fetal Lung lung
15 chr8:49059200-49060000 Enhancers NHEK skin
16 chr8:49059200-49060200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr8:49059200-49060200 Enhancers Osteobl bone
18 chr8:49059200-49060400 Enhancers Esophagus oesophagus
19 chr8:49059200-49060400 Enhancers HMEC breast
20 chr8:49059200-49060600 Enhancers Breast Myoepithelial Primary Cells Breast
21 chr8:49059200-49060600 Enhancers Liver Liver
22 chr8:49059200-49060600 Enhancers NHDF-Ad bronchial
23 chr8:49059200-49060800 Enhancers HepG2 liver
24 chr8:49059200-49061000 Enhancers Adipose Nuclei Adipose

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