Variant report

Variant rs73904704
Chromosome Location chr21:41501012-41501013
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:41491800-41510200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr21:41492400-41510400 Weak transcription Fetal Brain Female brain
3 chr21:41493000-41510200 Weak transcription Brain Angular Gyrus brain
4 chr21:41494200-41511600 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
5 chr21:41494800-41506000 Weak transcription Brain Cingulate Gyrus brain
6 chr21:41498400-41510200 Weak transcription Fetal Muscle Trunk muscle
7 chr21:41499000-41504600 Weak transcription Fetal Muscle Leg muscle
8 chr21:41499000-41517200 Strong transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr21:41499600-41503000 Enhancers HMEC breast
10 chr21:41500000-41503000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr21:41500400-41510600 Weak transcription Cortex derived primary cultured neurospheres brain
12 chr21:41500600-41501200 Weak transcription NHEK skin
13 chr21:41500600-41516200 Weak transcription Fetal Brain Male brain
14 chr21:41500800-41516200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr21:41501000-41502000 Enhancers Pancreatic Islets Pancreatic Islet

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