Variant report

Variant rs12591629
Chromosome Location chr15:76469024-76469025
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:76443200-76483000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
2 chr15:76463200-76469200 Weak transcription Left Ventricle heart
3 chr15:76463600-76469400 Weak transcription HSMMtube muscle
4 chr15:76464000-76469800 Weak transcription Placenta Amnion Placenta Amnion
5 chr15:76467600-76469600 Enhancers Psoas Muscle Psoas
6 chr15:76468000-76469400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr15:76468000-76478000 Weak transcription Pancreas Pancrea
8 chr15:76468400-76469200 Genic enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr15:76468400-76469600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
10 chr15:76468800-76469200 Flanking Active TSS Skeletal Muscle Female skeletal muscle
11 chr15:76468800-76471000 Enhancers Right Ventricle heart
12 chr15:76469000-76469200 Bivalent Enhancer Fetal Muscle Leg muscle
13 chr15:76469000-76469600 ZNF genes & repeats Foreskin Fibroblast Primary Cells skin01 Skin
14 chr15:76469000-76471000 Flanking Bivalent TSS/Enh Skeletal Muscle Male skeletal muscle

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