Variant report

Variant rs1400006
Chromosome Location chr2:182929224-182929225
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:182918800-182937400 Weak transcription Thymus Thymus
2 chr2:182926800-182929600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr2:182927200-182929400 Enhancers Fetal Intestine Small intestine
4 chr2:182928400-182929400 Enhancers Left Ventricle heart
5 chr2:182928400-182929600 Enhancers Fetal Intestine Large intestine
6 chr2:182928400-182929600 Enhancers Skeletal Muscle Male skeletal muscle
7 chr2:182928400-182930600 Enhancers Fetal Lung lung
8 chr2:182928400-182930600 Strong transcription Fetal Thymus thymus
9 chr2:182928600-182931600 Weak transcription Liver Liver
10 chr2:182928800-182929600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr2:182928800-182929600 Enhancers Fetal Heart heart
12 chr2:182929000-182929400 Enhancers Adipose Nuclei Adipose
13 chr2:182929000-182930200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr2:182929000-182930400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr2:182929000-182930400 Enhancers NHLF lung
16 chr2:182929200-182929400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
17 chr2:182929200-182929600 Enhancers Brain Cingulate Gyrus brain
18 chr2:182929200-182930000 Enhancers Pancreatic Islets Pancreatic Islet

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