Variant report

Variant rs4845541
Chromosome Location chr1:153360678-153360679
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr1:153356400-153361600 Enhancers Primary monocytes fromperipheralblood blood
3 chr1:153356800-153368200 Flanking Active TSS Primary neutrophils fromperipheralblood blood
4 chr1:153358000-153362800 Weak transcription Placenta Placenta
5 chr1:153359000-153360800 Enhancers Primary hematopoietic stem cells short term culture blood
6 chr1:153359800-153362400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr1:153360000-153362000 Weak transcription Esophagus oesophagus
8 chr1:153360000-153362000 Weak transcription HMEC breast
9 chr1:153360000-153362000 Weak transcription NHEK skin
10 chr1:153360000-153362400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr1:153360000-153362400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:153360200-153361600 Weak transcription Primary hematopoietic stem cells blood
13 chr1:153360400-153361800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:153360600-153360800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
15 chr1:153360600-153361200 Weak transcription Primary B cells from cord blood blood
16 chr1:153360600-153361400 Enhancers Monocytes-CD14+_RO01746 blood

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