Variant report

Variant rs569521330
Chromosome Location chr7:16358228-16358229
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16355600-16358400 Weak transcription A549 lung
2 chr7:16357200-16360400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr7:16357200-16372600 Weak transcription K562 blood
4 chr7:16357400-16358400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr7:16357800-16359800 Enhancers Stomach Mucosa stomach
6 chr7:16358200-16358600 Enhancers Gastric stomach
7 chr7:16358200-16359400 Enhancers HMEC breast
8 chr7:16358200-16359400 Enhancers NHEK skin
9 chr7:16358200-16359600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
10 chr7:16358200-16359600 Enhancers HUVEC blood vessel
11 chr7:16358200-16359600 Enhancers Osteobl bone
12 chr7:16358200-16359800 Enhancers NH-A brain

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