Variant report

Variant rs28469042
Chromosome Location chr2:211502131-211502132
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:211495200-211508000 Strong transcription Duodenum Mucosa Duodenum
2 chr2:211496200-211524800 Strong transcription Liver Liver
3 chr2:211496400-211504400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:211497400-211518000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
5 chr2:211498200-211529000 Strong transcription Hela-S3 cervix
6 chr2:211498800-211504200 Strong transcription Fetal Intestine Small intestine
7 chr2:211501000-211540600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:211501600-211503400 Enhancers HUES48 Cell Line embryonic stem cell
9 chr2:211501600-211503400 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr2:211501600-211508000 Strong transcription Fetal Intestine Large intestine
11 chr2:211501800-211502400 Enhancers ES-I3 Cell Line embryonic stem cell
12 chr2:211501800-211502800 Enhancers Breast Myoepithelial Primary Cells Breast

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