Variant report

Variant rs1415813
Chromosome Location chr20:22470776-22470777
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr20:22470000-22471000 Enhancers Liver Liver
3 chr20:22470000-22471000 Enhancers Fetal Intestine Large intestine
4 chr20:22470000-22472200 Enhancers Fetal Intestine Small intestine
5 chr20:22470200-22470800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr20:22470200-22472200 Flanking Active TSS HepG2 liver
7 chr20:22470400-22470800 Flanking Active TSS Rectal Mucosa Donor 29 rectum
8 chr20:22470400-22471000 Weak transcription Pancreas Pancrea
9 chr20:22470400-22472000 Enhancers HUES48 Cell Line embryonic stem cell
10 chr20:22470400-22472200 Flanking Active TSS A549 lung
11 chr20:22470600-22471000 Active TSS Duodenum Mucosa Duodenum
12 chr20:22470600-22471000 Enhancers Fetal Lung lung
13 chr20:22470600-22471000 Active TSS Rectal Mucosa Donor 31 rectum
14 chr20:22470600-22471200 Bivalent Enhancer Fetal Brain Female brain
15 chr20:22470600-22471200 Flanking Active TSS Stomach Mucosa stomach
16 chr20:22470600-22472000 Enhancers HUES6 Cell Line embryonic stem cell
17 chr20:22470600-22472200 Enhancers Fetal Kidney kidney
18 chr20:22470600-22472200 Active TSS Pancreatic Islets Pancreatic Islet

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