Variant report

Variant rs60006358
Chromosome Location chr4:3754951-3754952
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3748200-3758200 Weak transcription Aorta Aorta
2 chr4:3750000-3763200 Weak transcription Pancreas Pancrea
3 chr4:3752400-3755600 Bivalent Enhancer Fetal Muscle Trunk muscle
4 chr4:3753000-3756600 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
5 chr4:3753200-3755000 Bivalent Enhancer HepG2 liver
6 chr4:3753600-3755200 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr4:3753800-3756600 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr4:3753800-3756800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr4:3754400-3757000 Enhancers H1 Cell Line embryonic stem cell
10 chr4:3754600-3755400 Bivalent Enhancer Right Ventricle heart
11 chr4:3754800-3755000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
12 chr4:3754800-3756400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
13 chr4:3754800-3757000 Enhancers iPS-15b Cell Line embryonic stem cell

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