Variant report

Variant rs61803339
Chromosome Location chr1:153364926-153364927
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153353400-153366400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:153356800-153368200 Flanking Active TSS Primary neutrophils fromperipheralblood blood
3 chr1:153361600-153366400 Active TSS Primary hematopoietic stem cells blood
4 chr1:153361800-153368600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:153363200-153367400 Weak transcription Right Ventricle heart
6 chr1:153363600-153365600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
7 chr1:153364000-153366200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:153364000-153366200 Weak transcription Placenta Placenta
9 chr1:153364200-153366400 Active TSS Primary B cells from cord blood blood
10 chr1:153364400-153365000 Enhancers Esophagus oesophagus
11 chr1:153364400-153367000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr1:153364400-153367200 Weak transcription NHEK skin
13 chr1:153364400-153368200 Enhancers Primary monocytes fromperipheralblood blood
14 chr1:153364600-153365600 Weak transcription HMEC breast

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