Variant report

Variant rs997248
Chromosome Location chr1:84230245-84230246
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:84224800-84230600 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr1:84225000-84230400 Enhancers Primary B cells from cord blood blood
3 chr1:84226800-84230400 Enhancers Fetal Lung lung
4 chr1:84227800-84234600 Weak transcription Primary B cells from peripheral blood blood
5 chr1:84228400-84235400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr1:84229000-84230400 Enhancers Fetal Kidney kidney
7 chr1:84229200-84230400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr1:84229200-84230600 Weak transcription Adipose Nuclei Adipose
9 chr1:84229200-84231000 Enhancers HUES64 Cell Line embryonic stem cell
10 chr1:84229600-84231200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr1:84229600-84231400 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr1:84229800-84230800 Enhancers HUES48 Cell Line embryonic stem cell
13 chr1:84230000-84230400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr1:84230000-84230400 Enhancers Brain Germinal Matrix brain
15 chr1:84230000-84230600 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr1:84230000-84230600 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
17 chr1:84230000-84231000 Enhancers Liver Liver
18 chr1:84230000-84231200 Active TSS Pancreatic Islets Pancreatic Islet
19 chr1:84230000-84232000 Weak transcription Fetal Intestine Small intestine
20 chr1:84230000-84232200 Enhancers HepG2 liver
21 chr1:84230200-84230400 Enhancers HUES6 Cell Line embryonic stem cell
22 chr1:84230200-84230400 Enhancers iPS-15b Cell Line embryonic stem cell
23 chr1:84230200-84230400 Enhancers Fetal Brain Male brain

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