Variant report

Variant rs561884103
Chromosome Location chr4:3577635-3577636
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3550600-3580400 Weak transcription Right Atrium heart
2 chr4:3573000-3580200 ZNF genes & repeats ES-UCSF4 Cell Line embryonic stem cell
3 chr4:3573800-3578200 Enhancers Breast Myoepithelial Primary Cells Breast
4 chr4:3576000-3579600 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
5 chr4:3576600-3580200 Weak transcription Gastric stomach
6 chr4:3576800-3578600 Enhancers Fetal Intestine Large intestine
7 chr4:3577000-3578600 Enhancers Fetal Intestine Small intestine
8 chr4:3577400-3577800 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr4:3577400-3578000 Flanking Bivalent TSS/Enh HepG2 liver
10 chr4:3577600-3577800 Bivalent Enhancer H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr4:3577600-3577800 Bivalent Enhancer Right Ventricle heart
12 chr4:3577600-3578800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived

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