Variant report

Variant rs16844401
Chromosome Location chr4:3449652-3449653
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3437000-3450000 Weak transcription Brain Germinal Matrix brain
2 chr4:3437200-3451200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr4:3443200-3450600 Weak transcription Esophagus oesophagus
4 chr4:3443200-3451400 Weak transcription Fetal Lung lung
5 chr4:3445600-3451600 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr4:3445800-3451200 Weak transcription HepG2 liver
7 chr4:3445800-3453600 Weak transcription Skeletal Muscle Female skeletal muscle
8 chr4:3446600-3450800 Strong transcription Liver Liver
9 chr4:3448200-3450600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
10 chr4:3449000-3450000 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
11 chr4:3449000-3451000 Strong transcription Fetal Brain Female brain
12 chr4:3449200-3449800 Enhancers Pancreas Pancrea
13 chr4:3449600-3449800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
14 chr4:3449600-3452200 Weak transcription Spleen Spleen

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