Variant report

Variant rs73405628
Chromosome Location chr12:121027132-121027133
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:121019600-121027200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
2 chr12:121022800-121028800 Weak transcription Esophagus oesophagus
3 chr12:121023000-121027400 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr12:121026200-121027400 Enhancers Fetal Heart heart
5 chr12:121026200-121027600 Enhancers Fetal Muscle Leg muscle
6 chr12:121026400-121027600 Enhancers Fetal Muscle Trunk muscle
7 chr12:121026600-121027400 Flanking Active TSS Skeletal Muscle Female skeletal muscle
8 chr12:121026600-121027600 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr12:121026600-121027600 Enhancers Brain Dorsolateral Prefrontal Cortex brain
10 chr12:121026600-121027600 Enhancers Left Ventricle heart
11 chr12:121026600-121027600 Flanking Active TSS Skeletal Muscle Male skeletal muscle
12 chr12:121026800-121027400 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
13 chr12:121026800-121027400 Enhancers Psoas Muscle Psoas
14 chr12:121026800-121027400 Enhancers Right Ventricle heart
15 chr12:121026800-121027600 Enhancers HSMMtube muscle
16 chr12:121027000-121027200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr12:121027000-121027200 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
18 chr12:121027000-121027200 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin01 Skin
19 chr12:121027000-121027200 Enhancers Colonic Mucosa Colon
20 chr12:121027000-121027400 Enhancers Brain Anterior Caudate brain

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