Variant report

Variant rs71599064
Chromosome Location chr4:106565328-106565329
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:106545200-106577800 Weak transcription Pancreas Pancrea
2 chr4:106559200-106577800 Weak transcription Rectal Mucosa Donor 31 rectum
3 chr4:106559400-106576600 Weak transcription Fetal Intestine Large intestine
4 chr4:106559400-106580000 Weak transcription Sigmoid Colon Sigmoid Colon
5 chr4:106559400-106580200 Weak transcription Fetal Intestine Small intestine
6 chr4:106559400-106602800 Weak transcription Duodenum Mucosa Duodenum
7 chr4:106560000-106565600 Weak transcription Fetal Lung lung
8 chr4:106563400-106565400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
9 chr4:106565000-106565400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr4:106565200-106565800 Enhancers Cortex derived primary cultured neurospheres brain
11 chr4:106565200-106565800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr4:106565200-106566000 Enhancers NHEK skin

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