Variant report

Variant rs11889132
Chromosome Location chr2:21677263-21677264
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:21646800-21690600 Weak transcription Aorta Aorta
2 chr2:21674000-21677400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr2:21674000-21677400 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr2:21676200-21677400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr2:21676200-21678400 Weak transcription iPS-18 Cell Line embryonic stem cell
6 chr2:21676400-21678000 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr2:21676400-21679200 Weak transcription H1 Cell Line embryonic stem cell
8 chr2:21676600-21678000 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr2:21677000-21677400 Enhancers Rectal Smooth Muscle rectum
10 chr2:21677000-21677400 Flanking Active TSS NHLF lung
11 chr2:21677200-21677400 Enhancers HUES6 Cell Line embryonic stem cell
12 chr2:21677200-21677400 Enhancers Fetal Heart heart
13 chr2:21677200-21677400 Enhancers Ovary ovary

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