Variant report

Variant rs3014807
Chromosome Location chr1:153368020-153368021
allele A/C/G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153356800-153368200 Flanking Active TSS Primary neutrophils fromperipheralblood blood
2 chr1:153361800-153368600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:153364400-153368200 Enhancers Primary monocytes fromperipheralblood blood
4 chr1:153365400-153370200 Enhancers Esophagus oesophagus
5 chr1:153365600-153368400 Enhancers HMEC breast
6 chr1:153366200-153368200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:153367000-153371200 Enhancers Primary B cells from cord blood blood
8 chr1:153367200-153368200 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
9 chr1:153367200-153368200 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
10 chr1:153367200-153374800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
11 chr1:153367400-153368200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr1:153368000-153368200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr1:153368000-153368200 Bivalent Enhancer NHEK skin
14 chr1:153368000-153369000 Weak transcription Monocytes-CD14+_RO01746 blood

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