Variant report

Variant rs17098129
Chromosome Location chr14:32199504-32199505
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32171000-32200600 Weak transcription Placenta Amnion Placenta Amnion
2 chr14:32173400-32218000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr14:32174600-32200000 Weak transcription Primary T helper naive cells fromperipheralblood blood
4 chr14:32175400-32205600 Weak transcription Ovary ovary
5 chr14:32181400-32200600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr14:32186800-32205600 Weak transcription Primary T cells from cord blood blood
7 chr14:32195800-32200000 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr14:32198800-32200400 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr14:32199000-32201400 Weak transcription Primary T helper 17 cells PMA-I stimulated --
10 chr14:32199200-32201400 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr14:32199200-32210200 Weak transcription HepG2 liver
12 chr14:32199400-32199800 Strong transcription Primary T helper cells fromperipheralblood blood
13 chr14:32199400-32201200 ZNF genes & repeats Primary hematopoietic stem cells blood

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