Variant report

Variant rs535686973
Chromosome Location chr22:33855777-33855778
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:33828800-33857800 Weak transcription Primary B cells from peripheral blood blood
2 chr22:33848600-33857000 Weak transcription HepG2 liver
3 chr22:33848600-33860800 Weak transcription Fetal Lung lung
4 chr22:33852200-33860800 Weak transcription Pancreas Pancrea
5 chr22:33855000-33856200 Enhancers Gastric stomach
6 chr22:33855400-33857000 Enhancers Stomach Mucosa stomach
7 chr22:33855600-33856200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr22:33855600-33856600 Enhancers Fetal Heart heart
9 chr22:33855600-33856800 Enhancers Right Ventricle heart
10 chr22:33855600-33857000 Enhancers Left Ventricle heart

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