Variant report

Variant rs73902817
Chromosome Location chr20:22494060-22494061
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22490000-22496000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr20:22491800-22494400 Enhancers Fetal Intestine Large intestine
3 chr20:22492200-22494200 Flanking Active TSS HepG2 liver
4 chr20:22492200-22494400 Enhancers Fetal Intestine Small intestine
5 chr20:22492400-22494600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr20:22492400-22494600 Enhancers Stomach Mucosa stomach
7 chr20:22492600-22494200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr20:22492600-22494600 Enhancers Pancreas Pancrea
9 chr20:22493600-22494800 Enhancers Liver Liver
10 chr20:22493800-22494200 Enhancers A549 lung
11 chr20:22493800-22494800 Enhancers Pancreatic Islets Pancreatic Islet
12 chr20:22494000-22494200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr20:22494000-22494200 Bivalent Enhancer HUVEC blood vessel
14 chr20:22494000-22494600 Enhancers Rectal Mucosa Donor 31 rectum

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