Variant report

Variant rs13399063
Chromosome Location chr2:86042133-86042134
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:86024600-86043600 Weak transcription Right Ventricle heart
2 chr2:86029800-86054400 Weak transcription Spleen Spleen
3 chr2:86037600-86042600 Enhancers Skeletal Muscle Female skeletal muscle
4 chr2:86039000-86042400 Weak transcription Left Ventricle heart
5 chr2:86039800-86074800 Weak transcription Aorta Aorta
6 chr2:86040800-86042400 Enhancers Skeletal Muscle Male skeletal muscle
7 chr2:86040800-86042600 Enhancers A549 lung
8 chr2:86041000-86042200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr2:86041000-86042200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
10 chr2:86041000-86042600 Bivalent Enhancer Fetal Muscle Trunk muscle
11 chr2:86041000-86042600 Enhancers Pancreas Pancrea
12 chr2:86041200-86042200 Enhancers Cortex derived primary cultured neurospheres brain
13 chr2:86041200-86042400 Enhancers Brain Dorsolateral Prefrontal Cortex brain
14 chr2:86041400-86045200 Weak transcription Ovary ovary
15 chr2:86041400-86049600 Weak transcription Lung lung
16 chr2:86041800-86042200 Weak transcription Brain Anterior Caudate brain
17 chr2:86042000-86042200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
18 chr2:86042000-86042200 Bivalent Enhancer Fetal Muscle Leg muscle
19 chr2:86042000-86043400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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