Variant report

Variant rs376069882
Chromosome Location chr3:99513991-99513992
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:99492000-99517600 Weak transcription Stomach Smooth Muscle stomach
2 chr3:99502600-99518200 Weak transcription HSMMtube muscle
3 chr3:99502800-99518400 Weak transcription NH-A brain
4 chr3:99508400-99522200 Weak transcription NHDF-Ad bronchial
5 chr3:99508800-99518600 Strong transcription Osteobl bone
6 chr3:99510000-99523600 Weak transcription HUVEC blood vessel
7 chr3:99510400-99516200 Weak transcription NHLF lung
8 chr3:99510600-99515600 Weak transcription Skeletal Muscle Male skeletal muscle
9 chr3:99511800-99522800 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr3:99512600-99515000 Weak transcription Lung lung
11 chr3:99512800-99515400 Weak transcription Right Ventricle heart
12 chr3:99513000-99514600 Strong transcription NHEK skin
13 chr3:99513000-99514800 Strong transcription Aorta Aorta
14 chr3:99513000-99515000 Strong transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr3:99513000-99515000 Strong transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr3:99513000-99515200 Strong transcription HSMM muscle
17 chr3:99513000-99515800 Strong transcription Muscle Satellite Cultured Cells --
18 chr3:99513000-99518400 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
19 chr3:99513200-99514200 Strong transcription Foreskin Fibroblast Primary Cells skin01 Skin
20 chr3:99513200-99514600 Genic enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
21 chr3:99513200-99515800 Strong transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
22 chr3:99513600-99514600 Strong transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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