Variant report

Variant rs7278549
Chromosome Location chr21:39977656-39977657
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:39973000-39982000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr21:39976400-39977800 Enhancers iPS-20b Cell Line embryonic stem cell
3 chr21:39976600-39977800 Enhancers H1 Cell Line embryonic stem cell
4 chr21:39976600-39977800 Enhancers H9 Cell Line embryonic stem cell
5 chr21:39976600-39977800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
6 chr21:39976600-39978000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr21:39976800-39977800 Enhancers iPS-18 Cell Line embryonic stem cell
8 chr21:39977000-39977800 Enhancers HUES64 Cell Line embryonic stem cell
9 chr21:39977200-39978000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
10 chr21:39977400-39977800 Enhancers HUES6 Cell Line embryonic stem cell
11 chr21:39977600-39982200 Weak transcription Aorta Aorta

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