Variant report

Variant rs73490554
Chromosome Location chr11:67366805-67366806
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:67355000-67373200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr11:67355800-67368600 Weak transcription Rectal Mucosa Donor 29 rectum
3 chr11:67356200-67373800 Weak transcription Placenta Amnion Placenta Amnion
4 chr11:67366400-67367600 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr11:67366400-67367800 Enhancers K562 blood
6 chr11:67366600-67367600 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr11:67366800-67367000 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr11:67366800-67367000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr11:67366800-67367000 Enhancers Fetal Thymus thymus
10 chr11:67366800-67367800 Enhancers GM12878-XiMat blood
11 chr11:67366800-67368400 Enhancers Primary hematopoietic stem cells blood
12 chr11:67366800-67369000 Enhancers Primary neutrophils fromperipheralblood blood
13 chr11:67366800-67369400 Enhancers Primary Natural Killer cells fromperipheralblood blood

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