Variant report

Variant rs60170191
Chromosome Location chr22:22466731-22466732
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:22463800-22468200 Enhancers Primary B cells from peripheral blood blood
2 chr22:22464000-22466800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr22:22464400-22467000 Enhancers HMEC breast
4 chr22:22464600-22466800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
5 chr22:22464600-22467600 Enhancers Monocytes-CD14+_RO01746 blood
6 chr22:22465000-22467600 Enhancers Primary monocytes fromperipheralblood blood
7 chr22:22465000-22468400 Enhancers Primary neutrophils fromperipheralblood blood
8 chr22:22465400-22468400 Enhancers Primary B cells from cord blood blood
9 chr22:22465600-22472400 Weak transcription Esophagus oesophagus
10 chr22:22466000-22466800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr22:22466000-22470400 Weak transcription Right Atrium heart
12 chr22:22466200-22467600 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
13 chr22:22466400-22467000 Enhancers NHEK skin
14 chr22:22466400-22467800 Enhancers GM12878-XiMat blood
15 chr22:22466400-22468600 Enhancers K562 blood
16 chr22:22466600-22467800 Weak transcription Spleen Spleen

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