Variant report

Variant rs16975261
Chromosome Location chr13:110715607-110715608
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:110713800-110716200 Enhancers Liver Liver
2 chr13:110714000-110715800 Enhancers HMEC breast
3 chr13:110714000-110716000 Enhancers Pancreas Pancrea
4 chr13:110714000-110716200 Enhancers Right Ventricle heart
5 chr13:110714000-110716400 Enhancers Skeletal Muscle Female skeletal muscle
6 chr13:110714200-110715800 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr13:110714200-110716200 Enhancers HSMMtube muscle
8 chr13:110714400-110715800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr13:110714400-110716000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr13:110714400-110716200 Enhancers Left Ventricle heart
11 chr13:110714600-110716200 Enhancers Right Atrium heart
12 chr13:110714600-110716200 Enhancers HSMM muscle
13 chr13:110714800-110715800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr13:110715400-110715800 Enhancers Lung lung
15 chr13:110715400-110716000 Bivalent Enhancer Fetal Muscle Trunk muscle
16 chr13:110715400-110722200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr13:110715600-110716000 Enhancers Skeletal Muscle Male skeletal muscle

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