Variant report

Variant rs35178058
Chromosome Location chr1:184112428-184112429
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:184109600-184115600 Enhancers Fetal Brain Male brain
2 chr1:184111800-184113800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
3 chr1:184111800-184113800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:184111800-184114400 Enhancers Fetal Muscle Leg muscle
5 chr1:184112200-184113200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
6 chr1:184112200-184113200 Enhancers Skeletal Muscle Male skeletal muscle
7 chr1:184112200-184113200 Enhancers Stomach Smooth Muscle stomach
8 chr1:184112200-184114600 Enhancers Fetal Brain Female brain
9 chr1:184112400-184112600 Enhancers HSMMtube muscle
10 chr1:184112400-184112600 Enhancers NHLF lung
11 chr1:184112400-184112600 Enhancers Osteobl bone
12 chr1:184112400-184113000 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr1:184112400-184113000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr1:184112400-184113000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr1:184112400-184113200 Enhancers Left Ventricle heart
16 chr1:184112400-184113200 Enhancers NHDF-Ad bronchial
17 chr1:184112400-184113400 Enhancers Fetal Heart heart
18 chr1:184112400-184113400 Enhancers Skeletal Muscle Female skeletal muscle

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