Variant report

Variant rs59096149
Chromosome Location chr16:81273869-81273870
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:81272200-81274200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr16:81272400-81274200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr16:81272400-81275200 Weak transcription Esophagus oesophagus
4 chr16:81272600-81276800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr16:81272600-81276800 Weak transcription NHEK skin
6 chr16:81272600-81277200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr16:81272600-81277400 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr16:81272600-81286400 Weak transcription Right Atrium heart
9 chr16:81273000-81277600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr16:81273400-81277400 Weak transcription HUES6 Cell Line embryonic stem cell
11 chr16:81273600-81277000 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr16:81273600-81277400 Weak transcription H1 Cell Line embryonic stem cell
13 chr16:81273600-81299400 Weak transcription Duodenum Mucosa Duodenum

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