Variant report

Variant rs546131
Chromosome Location chr11:34851760-34851761
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:34847000-34852000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr11:34847200-34858400 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr11:34847400-34852200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr11:34847600-34852000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr11:34847800-34851800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
6 chr11:34848200-34854400 Weak transcription Esophagus oesophagus
7 chr11:34851400-34852000 Enhancers HepG2 liver
8 chr11:34851400-34852200 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr11:34851400-34852200 Enhancers Hela-S3 cervix
10 chr11:34851400-34853200 Enhancers K562 blood
11 chr11:34851600-34852400 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr11:34851600-34852400 Enhancers Breast Myoepithelial Primary Cells Breast
13 chr11:34851600-34852600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr11:34851600-34852600 Enhancers Right Ventricle heart
15 chr11:34851600-34852800 Enhancers Fetal Heart heart

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