Variant report

Variant rs4845346
Chromosome Location chr1:153367113-153367114
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 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 chr1:153363200-153367400 Weak transcription Right Ventricle heart
4 chr1:153364400-153367200 Weak transcription NHEK skin
5 chr1:153364400-153368200 Enhancers Primary monocytes fromperipheralblood blood
6 chr1:153365400-153370200 Enhancers Esophagus oesophagus
7 chr1:153365600-153368000 Enhancers Monocytes-CD14+_RO01746 blood
8 chr1:153365600-153368400 Enhancers HMEC breast
9 chr1:153366200-153367400 Enhancers Placenta Placenta
10 chr1:153366200-153368200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:153366400-153367200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr1:153367000-153367200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr1:153367000-153371200 Enhancers Primary B cells from cord blood blood

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