Variant report

Variant rs58106116
Chromosome Location chr2:21676486-21676487
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:21646800-21690600 Weak transcription Aorta Aorta
2 chr2:21672600-21677000 Weak transcription Rectal Smooth Muscle rectum
3 chr2:21674000-21677400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr2:21674000-21677400 Enhancers Fetal Adrenal Gland Adrenal Gland
5 chr2:21674800-21676600 Enhancers iPS-20b Cell Line embryonic stem cell
6 chr2:21675000-21676800 Enhancers HUES6 Cell Line embryonic stem cell
7 chr2:21675200-21676800 Enhancers Duodenum Smooth Muscle Duodenum
8 chr2:21675600-21676600 Enhancers Ovary ovary
9 chr2:21675600-21677200 Enhancers Stomach Smooth Muscle stomach
10 chr2:21676200-21677400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
11 chr2:21676200-21678400 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr2:21676400-21676600 Enhancers Fetal Heart heart
13 chr2:21676400-21676600 Flanking Active TSS NHLF lung
14 chr2:21676400-21678000 Weak transcription HUES48 Cell Line embryonic stem cell
15 chr2:21676400-21679200 Weak transcription H1 Cell Line embryonic stem cell

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