Variant report

Variant rs66905067
Chromosome Location chr1:211772400-211772401
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211757400-211775200 Weak transcription Fetal Intestine Small intestine
2 chr1:211768600-211772400 Enhancers Primary hematopoietic stem cells short term culture blood
3 chr1:211770200-211775200 Weak transcription Fetal Intestine Large intestine
4 chr1:211770600-211773000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:211770600-211775400 Weak transcription Liver Liver
6 chr1:211771600-211772400 Weak transcription GM12878-XiMat blood
7 chr1:211771600-211775400 Weak transcription Primary neutrophils fromperipheralblood blood
8 chr1:211771600-211786200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:211771800-211775200 Weak transcription NHDF-Ad bronchial
10 chr1:211771800-211775400 Weak transcription Primary monocytes fromperipheralblood blood
11 chr1:211771800-211775400 Weak transcription Monocytes-CD14+_RO01746 blood
12 chr1:211771800-211775600 Weak transcription NHLF lung
13 chr1:211771800-211776000 Weak transcription Osteobl bone
14 chr1:211772200-211773200 Enhancers HepG2 liver
15 chr1:211772200-211773200 Enhancers K562 blood
16 chr1:211772200-211778000 Enhancers Placenta Placenta
17 chr1:211772400-211775400 Weak transcription Primary hematopoietic stem cells short term culture blood

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