Variant report

Variant rs11087380
Chromosome Location chr20:22472098-22472099
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:22469800-22475400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr20:22470000-22472200 Enhancers Fetal Intestine Small intestine
3 chr20:22470200-22472200 Flanking Active TSS HepG2 liver
4 chr20:22470400-22472200 Flanking Active TSS A549 lung
5 chr20:22470600-22472200 Enhancers Fetal Kidney kidney
6 chr20:22470600-22472200 Active TSS Pancreatic Islets Pancreatic Islet
7 chr20:22471200-22473600 Enhancers Liver Liver
8 chr20:22471200-22473600 Enhancers Stomach Mucosa stomach
9 chr20:22471400-22475400 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr20:22471600-22472200 Enhancers Fetal Intestine Large intestine
11 chr20:22471800-22475600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr20:22472000-22472200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr20:22472000-22472400 Enhancers Rectal Mucosa Donor 31 rectum
14 chr20:22472000-22473200 Weak transcription Pancreas Pancrea
15 chr20:22472000-22475400 Weak transcription HUES6 Cell Line embryonic stem cell
16 chr20:22472000-22475600 Weak transcription HUES64 Cell Line embryonic stem cell

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