Variant report

Variant rs11824860
Chromosome Location chr11:70576477-70576478
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:70560000-70577400 Weak transcription HepG2 liver
2 chr11:70560200-70588200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr11:70560400-70588200 Weak transcription H9 Cell Line embryonic stem cell
4 chr11:70566800-70577800 Weak transcription Fetal Intestine Small intestine
5 chr11:70571600-70579000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
6 chr11:70572400-70578000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr11:70574600-70578800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr11:70574800-70580200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr11:70575000-70592400 Weak transcription Right Atrium heart
10 chr11:70576200-70576800 Enhancers Gastric stomach
11 chr11:70576400-70576600 Active TSS H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr11:70576400-70576600 Enhancers Pancreas Pancrea
13 chr11:70576400-70576800 Enhancers Duodenum Mucosa Duodenum

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