Variant report

Variant rs9469513
Chromosome Location chr6:33533866-33533867
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:33516800-33537600 Weak transcription Primary T cells fromperipheralblood blood
2 chr6:33530400-33534400 Weak transcription HMEC breast
3 chr6:33530400-33534600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr6:33530400-33536800 Weak transcription K562 blood
5 chr6:33530400-33537600 Weak transcription GM12878-XiMat blood
6 chr6:33530400-33538800 Weak transcription Esophagus oesophagus
7 chr6:33531000-33538200 Weak transcription Primary T cells from cord blood blood
8 chr6:33531400-33538400 Weak transcription Osteobl bone
9 chr6:33533200-33538400 Weak transcription Primary hematopoietic stem cells short term culture blood
10 chr6:33533200-33538600 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr6:33533600-33535800 Weak transcription Fetal Stomach stomach
12 chr6:33533600-33537600 Weak transcription Fetal Thymus thymus
13 chr6:33533800-33535400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr6:33533800-33536000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr6:33533800-33538400 Weak transcription Rectal Smooth Muscle rectum

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