Variant report

Variant rs537248778
Chromosome Location chr11:16320542-16320543
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16302200-16321600 Weak transcription Left Ventricle heart
2 chr11:16313400-16322200 Enhancers Brain Germinal Matrix brain
3 chr11:16315200-16351800 Weak transcription Fetal Intestine Large intestine
4 chr11:16315600-16321600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr11:16315600-16322200 Weak transcription Fetal Kidney kidney
6 chr11:16317400-16327400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:16319400-16321400 Weak transcription Pancreas Pancrea
8 chr11:16319400-16321600 Weak transcription Cortex derived primary cultured neurospheres brain
9 chr11:16319400-16321600 Weak transcription Fetal Muscle Leg muscle
10 chr11:16319400-16322000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr11:16319400-16377600 Weak transcription Psoas Muscle Psoas
12 chr11:16319600-16320600 Enhancers Pancreatic Islets Pancreatic Islet
13 chr11:16319600-16320800 Weak transcription K562 blood
14 chr11:16319600-16321400 Weak transcription Skeletal Muscle Female skeletal muscle
15 chr11:16319600-16321800 Weak transcription Fetal Lung lung
16 chr11:16319600-16321800 Weak transcription Skeletal Muscle Male skeletal muscle
17 chr11:16319800-16321200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
18 chr11:16320400-16320600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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