Variant report

Variant rs3985603
Chromosome Location chr11:16283644-16283645
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16271400-16289200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr11:16271800-16286400 Weak transcription Psoas Muscle Psoas
3 chr11:16279600-16300400 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr11:16283600-16283800 Active TSS Pancreatic Islets Pancreatic Islet
5 chr11:16283600-16284400 Enhancers Fetal Intestine Small intestine
6 chr11:16283600-16284400 Enhancers A549 lung
7 chr11:16283600-16284400 Flanking Active TSS HepG2 liver
8 chr11:16283600-16284600 Enhancers Fetal Intestine Large intestine
9 chr11:16283600-16284600 Enhancers Rectal Mucosa Donor 31 rectum
10 chr11:16283600-16285000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr11:16283600-16285200 Enhancers Liver Liver

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