Variant report

Variant rs6659104
Chromosome Location chr1:153362146-153362147
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr1:153358000-153362800 Weak transcription Placenta Placenta
4 chr1:153359800-153362400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:153360000-153362400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr1:153360000-153362400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:153360800-153362400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:153361200-153363800 Active TSS Primary B cells from cord blood blood
9 chr1:153361400-153363000 Flanking Active TSS Monocytes-CD14+_RO01746 blood
10 chr1:153361600-153362400 Enhancers Primary mononuclear cells fromperipheralblood Blood
11 chr1:153361600-153362600 Flanking Active TSS Primary monocytes fromperipheralblood blood
12 chr1:153361600-153366400 Active TSS Primary hematopoietic stem cells blood
13 chr1:153361800-153368600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:153362000-153362200 Flanking Active TSS Esophagus oesophagus
15 chr1:153362000-153362200 Enhancers Spleen Spleen
16 chr1:153362000-153362800 Enhancers Primary hematopoietic stem cells short term culture blood
17 chr1:153362000-153364400 Enhancers NHEK skin
18 chr1:153362000-153364600 Enhancers HMEC breast

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