Variant report

Variant rs79971467
Chromosome Location chr1:56829253-56829254
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:56825400-56829600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:56825400-56839000 Weak transcription Psoas Muscle Psoas
3 chr1:56827800-56829600 Enhancers Skeletal Muscle Female skeletal muscle
4 chr1:56827800-56830000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr1:56827800-56830000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:56828000-56829600 Enhancers Brain Cingulate Gyrus brain
7 chr1:56828000-56829800 Enhancers Brain Hippocampus Middle brain
8 chr1:56828200-56829600 Enhancers Cortex derived primary cultured neurospheres brain
9 chr1:56828600-56829600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
10 chr1:56828600-56829800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr1:56828600-56829800 Enhancers Brain Anterior Caudate brain
12 chr1:56828600-56829800 Enhancers Brain Inferior Temporal Lobe brain
13 chr1:56828800-56829400 Enhancers Skeletal Muscle Male skeletal muscle
14 chr1:56828800-56829600 Enhancers Brain Substantia Nigra brain
15 chr1:56828800-56829800 Enhancers HepG2 liver
16 chr1:56829000-56829400 Enhancers HUES64 Cell Line embryonic stem cell
17 chr1:56829000-56829400 Enhancers Left Ventricle heart
18 chr1:56829000-56829800 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived

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