Variant report

Variant rs535791095
Chromosome Location chr2:145441066-145441067
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:145438800-145452800 Enhancers Primary monocytes fromperipheralblood blood
2 chr2:145439400-145442000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr2:145440000-145441200 Enhancers Fetal Lung lung
4 chr2:145440000-145441600 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
5 chr2:145440000-145441600 Enhancers Ovary ovary
6 chr2:145440000-145442000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
7 chr2:145440000-145442400 Enhancers Primary hematopoietic stem cells short term culture blood
8 chr2:145440200-145442200 Flanking Active TSS Monocytes-CD14+_RO01746 blood
9 chr2:145440400-145441800 Enhancers K562 blood
10 chr2:145440600-145441800 Enhancers Primary B cells from peripheral blood blood
11 chr2:145440600-145441800 Enhancers Adipose Nuclei Adipose
12 chr2:145440600-145441800 Enhancers Colon Smooth Muscle Colon
13 chr2:145440600-145442000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
14 chr2:145440600-145442200 Enhancers Primary hematopoietic stem cells blood
15 chr2:145440800-145441600 Enhancers Aorta Aorta
16 chr2:145440800-145441600 Weak transcription Duodenum Smooth Muscle Duodenum
17 chr2:145440800-145442000 Flanking Active TSS Primary B cells from cord blood blood
18 chr2:145440800-145442000 Enhancers Fetal Kidney kidney
19 chr2:145440800-145442600 Enhancers Primary neutrophils fromperipheralblood blood

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