Variant report

Variant rs7564341
Chromosome Location chr2:144561589-144561590
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:144553800-144564000 Weak transcription HUES6 Cell Line embryonic stem cell
2 chr2:144559200-144561800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
3 chr2:144559200-144562000 Enhancers Fetal Lung lung
4 chr2:144559400-144564000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr2:144560000-144563200 Enhancers Fetal Stomach stomach
6 chr2:144560400-144562000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr2:144561200-144562000 Enhancers Fetal Heart heart
8 chr2:144561400-144561600 Enhancers GM12878-XiMat blood
9 chr2:144561400-144565400 Weak transcription Right Atrium heart
10 chr2:144561400-144565400 Weak transcription NHLF lung

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