Variant report

Variant rs61840453
Chromosome Location chr1:246330591-246330592
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246314200-246369000 Weak transcription Aorta Aorta
2 chr1:246321600-246344000 Weak transcription Primary hematopoietic stem cells blood
3 chr1:246325600-246342000 Weak transcription Primary T cells from cord blood blood
4 chr1:246326200-246339600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:246327200-246340200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:246327400-246332200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr1:246327600-246341600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:246329000-246341800 Weak transcription Monocytes-CD14+_RO01746 blood
9 chr1:246329400-246330600 Flanking Active TSS NHEK skin
10 chr1:246329800-246330800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr1:246329800-246330800 Strong transcription Osteobl bone
12 chr1:246330000-246330600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr1:246330000-246330600 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr1:246330400-246332000 Weak transcription HepG2 liver
15 chr1:246330400-246332000 Enhancers K562 blood

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