Variant report

Variant rs1203906
Chromosome Location chr20:22560921-22560922
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22559200-22562200 Weak transcription Gastric stomach
2 chr20:22560000-22561200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
3 chr20:22560200-22561400 Genic enhancers A549 lung
4 chr20:22560400-22561000 Bivalent Enhancer Fetal Lung lung
5 chr20:22560400-22561000 Bivalent Enhancer Stomach Mucosa stomach
6 chr20:22560400-22561200 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
7 chr20:22560400-22561200 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
8 chr20:22560600-22561200 Bivalent Enhancer HUES48 Cell Line embryonic stem cell
9 chr20:22560600-22561200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
10 chr20:22560600-22561200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
11 chr20:22560600-22561200 Flanking Bivalent TSS/Enh Rectal Mucosa Donor 31 rectum
12 chr20:22560600-22563400 Transcr. at gene 5' and 3' hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr20:22560800-22561200 Flanking Active TSS Pancreas Pancrea
14 chr20:22560800-22561400 Flanking Active TSS Liver Liver
15 chr20:22560800-22561600 Flanking Active TSS Pancreatic Islets Pancreatic Islet
16 chr20:22560800-22562200 Genic enhancers HepG2 liver

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