Variant report

Variant rs9646799
Chromosome Location chr2:182241698-182241699
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:182237600-182248400 Weak transcription Primary T cells from cord blood blood
2 chr2:182237800-182243400 Weak transcription Thymus Thymus
3 chr2:182237800-182249600 Weak transcription Primary T helper cells PMA-I stimulated --
4 chr2:182238000-182258200 Weak transcription Primary T helper cells fromperipheralblood blood
5 chr2:182240000-182247400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr2:182240000-182257400 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
7 chr2:182240200-182245400 Weak transcription Primary hematopoietic stem cells blood
8 chr2:182240200-182245400 Weak transcription Adipose Nuclei Adipose
9 chr2:182240800-182241800 Enhancers GM12878-XiMat blood
10 chr2:182241400-182242800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
11 chr2:182241400-182245400 Weak transcription Pancreas Pancrea
12 chr2:182241400-182245400 Weak transcription NHDF-Ad bronchial
13 chr2:182241600-182241800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr2:182241600-182245400 Weak transcription Dnd41 blood
15 chr2:182241600-182258200 Weak transcription Fetal Thymus thymus

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