Variant report

Variant rs374914059
Chromosome Location chr6:114066000-114066001
allele A/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:114064200-114066200 Weak transcription Fetal Heart heart
2 chr6:114065000-114067800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr6:114065800-114066000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr6:114065800-114066400 Enhancers Pancreatic Islets Pancreatic Islet
5 chr6:114065800-114066400 Enhancers Fetal Lung lung
6 chr6:114065800-114066400 Enhancers Fetal Muscle Leg muscle
7 chr6:114065800-114066400 Enhancers Placenta Placenta
8 chr6:114065800-114066400 Enhancers HepG2 liver
9 chr6:114065800-114066800 Enhancers Adipose Nuclei Adipose
10 chr6:114065800-114067200 Enhancers Psoas Muscle Psoas
11 chr6:114065800-114067200 Enhancers Skeletal Muscle Female skeletal muscle
12 chr6:114066000-114066400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr6:114066000-114066600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr6:114066000-114066800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr6:114066000-114067000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr6:114066000-114067200 Enhancers Colon Smooth Muscle Colon
17 chr6:114066000-114067200 Enhancers Skeletal Muscle Male skeletal muscle

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