Variant report

Variant rs11208911
Chromosome Location chr1:67048489-67048490
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:67041600-67062400 Weak transcription Stomach Smooth Muscle stomach
2 chr1:67043200-67052000 Weak transcription Brain Angular Gyrus brain
3 chr1:67043200-67056800 Weak transcription Brain Anterior Caudate brain
4 chr1:67043200-67064400 Weak transcription Brain Inferior Temporal Lobe brain
5 chr1:67043400-67056200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr1:67043600-67050600 Weak transcription Brain Hippocampus Middle brain
7 chr1:67043600-67066600 Weak transcription Fetal Brain Male brain
8 chr1:67044000-67057200 Weak transcription Aorta Aorta
9 chr1:67044200-67064000 Weak transcription NH-A brain
10 chr1:67044800-67050600 Weak transcription NHDF-Ad bronchial
11 chr1:67044800-67064000 Weak transcription Osteobl bone
12 chr1:67045000-67050400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr1:67045000-67050600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:67045000-67050600 Weak transcription Muscle Satellite Cultured Cells --
15 chr1:67045600-67056000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
16 chr1:67046000-67049400 Weak transcription Psoas Muscle Psoas
17 chr1:67046400-67060400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
18 chr1:67047600-67048600 Enhancers Fetal Lung lung
19 chr1:67048200-67049000 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung

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