Variant report

Variant rs16844394
Chromosome Location chr4:3448852-3448853
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3436600-3449000 Weak transcription Fetal Brain Female brain
2 chr4:3437000-3450000 Weak transcription Brain Germinal Matrix brain
3 chr4:3437200-3451200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr4:3443200-3450600 Weak transcription Esophagus oesophagus
5 chr4:3443200-3451400 Weak transcription Fetal Lung lung
6 chr4:3445600-3449200 Weak transcription Pancreas Pancrea
7 chr4:3445600-3451600 Weak transcription Primary hematopoietic stem cells short term culture blood
8 chr4:3445800-3451200 Weak transcription HepG2 liver
9 chr4:3445800-3453600 Weak transcription Skeletal Muscle Female skeletal muscle
10 chr4:3446400-3449600 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr4:3446600-3450800 Strong transcription Liver Liver
12 chr4:3448200-3450600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr4:3448600-3449000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
14 chr4:3448800-3449000 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin01 Skin
15 chr4:3448800-3449600 ZNF genes & repeats Spleen Spleen

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