Variant report

Variant rs547459944
Chromosome Location chr3:139001464-139001465
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:138999000-139006800 Weak transcription Pancreas Pancrea
2 chr3:138999200-139001800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr3:139000000-139001600 Flanking Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
4 chr3:139000000-139001800 Flanking Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
5 chr3:139000600-139001600 Enhancers Left Ventricle heart
6 chr3:139000600-139003000 Flanking Active TSS NHDF-Ad bronchial
7 chr3:139000800-139002600 Enhancers K562 blood
8 chr3:139000800-139004400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr3:139000800-139011200 Weak transcription NHLF lung
10 chr3:139001000-139001600 Enhancers Brain Dorsolateral Prefrontal Cortex brain
11 chr3:139001200-139001800 Enhancers Brain Substantia Nigra brain
12 chr3:139001200-139002800 Weak transcription Ovary ovary
13 chr3:139001200-139003200 Enhancers Brain Cingulate Gyrus brain
14 chr3:139001200-139003200 Enhancers Brain Hippocampus Middle brain
15 chr3:139001200-139004600 Weak transcription Right Ventricle heart
16 chr3:139001400-139001600 Flanking Active TSS HSMM muscle
17 chr3:139001400-139001800 Enhancers Brain Inferior Temporal Lobe brain
18 chr3:139001400-139003200 Enhancers Brain Angular Gyrus brain

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