Variant report

Variant rs574928995
Chromosome Location chr1:174797861-174797862
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174777600-174799800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr1:174782000-174800800 Weak transcription Duodenum Mucosa Duodenum
3 chr1:174782200-174813000 Weak transcription Primary T regulatory cells fromperipheralblood blood
4 chr1:174782600-174799200 Weak transcription Liver Liver
5 chr1:174784800-174806600 Weak transcription HSMMtube muscle
6 chr1:174786800-174798200 Weak transcription Left Ventricle heart
7 chr1:174792600-174801600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr1:174796600-174833400 Weak transcription Primary B cells from cord blood blood
9 chr1:174797200-174798400 Enhancers HMEC breast
10 chr1:174797400-174798000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:174797400-174798400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:174797400-174798400 Enhancers NHEK skin
13 chr1:174797800-174798400 Strong transcription GM12878-XiMat blood

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