Variant report

Variant rs10450783
Chromosome Location chr12:48418146-48418147
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:48415000-48418200 Enhancers Fetal Intestine Large intestine
2 chr12:48415000-48418200 Enhancers Fetal Intestine Small intestine
3 chr12:48415200-48418200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr12:48415800-48420400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr12:48416800-48418200 Enhancers Skeletal Muscle Male skeletal muscle
6 chr12:48416800-48423400 Weak transcription Right Atrium heart
7 chr12:48417000-48418600 Weak transcription Right Ventricle heart
8 chr12:48417400-48419000 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell
9 chr12:48417600-48418200 Enhancers Skeletal Muscle Female skeletal muscle
10 chr12:48417600-48420800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
11 chr12:48417800-48418200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr12:48417800-48419200 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr12:48417800-48421400 Weak transcription Rectal Mucosa Donor 31 rectum
14 chr12:48417800-48423400 Weak transcription Fetal Lung lung
15 chr12:48418000-48418400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr12:48418000-48419000 Weak transcription HepG2 liver
17 chr12:48418000-48420200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
18 chr12:48418000-48422200 Weak transcription Fetal Heart heart

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