Variant report

Variant rs374429556
Chromosome Location chr11:3603056-3603057
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:3601400-3603200 Active TSS Fetal Intestine Large intestine
2 chr11:3602400-3603400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr11:3602400-3603400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
4 chr11:3602600-3604200 Bivalent Enhancer H1 Cell Line embryonic stem cell
5 chr11:3602800-3603200 Enhancers Duodenum Mucosa Duodenum
6 chr11:3602800-3603200 Enhancers Fetal Intestine Small intestine
7 chr11:3602800-3603400 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
8 chr11:3602800-3603600 Enhancers H9 Cell Line embryonic stem cell
9 chr11:3602800-3603600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
10 chr11:3602800-3604000 Weak transcription ES-WA7 Cell Line embryonic stem cell
11 chr11:3602800-3604800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr11:3602800-3605200 Weak transcription Lung lung
13 chr11:3602800-3605800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr11:3603000-3604000 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived

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