Variant report

Variant rs56077417
Chromosome Location chr11:16140423-16140424
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16133800-16141600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr11:16133800-16146400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr11:16136800-16144000 Weak transcription Pancreatic Islets Pancreatic Islet
4 chr11:16137400-16140600 Weak transcription Fetal Heart heart
5 chr11:16137400-16146600 Weak transcription Pancreas Pancrea
6 chr11:16138800-16147600 Weak transcription Fetal Intestine Small intestine
7 chr11:16139200-16141600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr11:16139400-16141800 Enhancers Cortex derived primary cultured neurospheres brain
9 chr11:16139600-16141200 Enhancers Fetal Lung lung
10 chr11:16139600-16141400 Enhancers Skeletal Muscle Male skeletal muscle
11 chr11:16139800-16140600 Enhancers Fetal Kidney kidney
12 chr11:16140200-16141000 Weak transcription Brain Germinal Matrix brain
13 chr11:16140200-16141200 Weak transcription HepG2 liver
14 chr11:16140200-16148000 Weak transcription Psoas Muscle Psoas

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