Variant report

Variant rs35350728
Chromosome Location chr11:16142437-16142438
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16133800-16146400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr11:16136800-16144000 Weak transcription Pancreatic Islets Pancreatic Islet
3 chr11:16137400-16146600 Weak transcription Pancreas Pancrea
4 chr11:16138800-16147600 Weak transcription Fetal Intestine Small intestine
5 chr11:16140200-16148000 Weak transcription Psoas Muscle Psoas
6 chr11:16141200-16147400 Weak transcription Brain Germinal Matrix brain
7 chr11:16141200-16147800 Weak transcription Fetal Heart heart
8 chr11:16141400-16145800 Weak transcription HepG2 liver
9 chr11:16141400-16147600 Weak transcription Skeletal Muscle Male skeletal muscle
10 chr11:16141800-16143800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr11:16142000-16143400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell

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