Variant report

Variant rs58775468
Chromosome Location chr12:4217991-4217992
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:4216000-4224000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr12:4216400-4218600 Enhancers Primary monocytes fromperipheralblood blood
3 chr12:4216600-4224000 Weak transcription Primary hematopoietic stem cells short term culture blood
4 chr12:4216800-4225000 Weak transcription Placenta Amnion Placenta Amnion
5 chr12:4217000-4218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:4217000-4219600 Enhancers GM12878-XiMat blood
7 chr12:4217000-4220000 Weak transcription Duodenum Mucosa Duodenum
8 chr12:4217000-4220400 Weak transcription Primary neutrophils fromperipheralblood blood
9 chr12:4217000-4221400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
10 chr12:4217000-4222200 Weak transcription Fetal Thymus thymus
11 chr12:4217000-4223800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr12:4217000-4224000 Weak transcription Primary T regulatory cells fromperipheralblood blood
13 chr12:4217200-4220600 Weak transcription Monocytes-CD14+_RO01746 blood
14 chr12:4217600-4219400 Enhancers HMEC breast
15 chr12:4217600-4219400 Enhancers NHEK skin
16 chr12:4217800-4219200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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