Variant report

Variant rs11822790
Chromosome Location chr11:16263355-16263356
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16248200-16274200 Weak transcription Pancreas Pancrea
2 chr11:16256200-16272000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
3 chr11:16258600-16264200 Enhancers Fetal Heart heart
4 chr11:16262000-16263800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr11:16262400-16268000 Weak transcription Cortex derived primary cultured neurospheres brain
6 chr11:16262800-16263800 Enhancers Fetal Brain Female brain
7 chr11:16262800-16264200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
8 chr11:16263200-16263400 Enhancers Fetal Muscle Leg muscle
9 chr11:16263200-16263400 Enhancers Left Ventricle heart
10 chr11:16263200-16263400 Enhancers Psoas Muscle Psoas
11 chr11:16263200-16263400 Enhancers Right Atrium heart
12 chr11:16263200-16263800 Enhancers Skeletal Muscle Male skeletal muscle
13 chr11:16263200-16264000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr11:16263200-16264000 Enhancers Right Ventricle heart
15 chr11:16263200-16264000 Enhancers Skeletal Muscle Female skeletal muscle

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