Variant report

Variant rs6746186
Chromosome Location chr2:7249578-7249579
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:7234800-7249800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr2:7238000-7252000 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr2:7238000-7259000 Weak transcription Brain Anterior Caudate brain
4 chr2:7238000-7259600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr2:7238000-7260400 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr2:7238200-7249600 Weak transcription Fetal Muscle Leg muscle
7 chr2:7238200-7258800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
8 chr2:7245600-7253400 Weak transcription Dnd41 blood
9 chr2:7246600-7266400 Weak transcription Primary T cells from cord blood blood
10 chr2:7249400-7249800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr2:7249400-7249800 Enhancers Fetal Brain Female brain
12 chr2:7249400-7250000 Enhancers Primary hematopoietic stem cells blood
13 chr2:7249400-7250000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
14 chr2:7249400-7250000 Enhancers Fetal Brain Male brain
15 chr2:7249400-7250400 Enhancers Fetal Kidney kidney

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