Variant report

Variant rs4488885
Chromosome Location chr4:3285953-3285954
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:3272400-3287600 Weak transcription Pancreas Pancrea
2 chr4:3284800-3286600 Enhancers HepG2 liver
3 chr4:3284800-3287600 Weak transcription NHDF-Ad bronchial
4 chr4:3285000-3286800 Weak transcription Primary monocytes fromperipheralblood blood
5 chr4:3285400-3286200 Bivalent Enhancer Fetal Muscle Trunk muscle
6 chr4:3285600-3286000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin02 Skin
7 chr4:3285600-3286200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr4:3285800-3286000 Enhancers Breast Myoepithelial Primary Cells Breast
9 chr4:3285800-3286000 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr4:3285800-3286000 Enhancers HMEC breast
11 chr4:3285800-3287800 Weak transcription Fetal Brain Female brain

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