Variant report

Variant rs17880109
Chromosome Location chr11:102668372-102668373
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:102655600-102668600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr11:102662200-102668400 Weak transcription NHLF lung
3 chr11:102663000-102668600 Weak transcription NHEK skin
4 chr11:102664200-102668800 Active TSS Foreskin Fibroblast Primary Cells skin02 Skin
5 chr11:102665200-102669400 Weak transcription Duodenum Mucosa Duodenum
6 chr11:102665400-102668400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr11:102665400-102668400 Weak transcription HMEC breast
8 chr11:102665400-102672000 Weak transcription Fetal Stomach stomach
9 chr11:102667400-102668600 Active TSS HUVEC blood vessel
10 chr11:102667600-102671200 Enhancers Fetal Intestine Small intestine
11 chr11:102667800-102668400 Active TSS Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr11:102667800-102671000 Enhancers Stomach Mucosa stomach
13 chr11:102668000-102670000 Enhancers Lung lung
14 chr11:102668000-102670400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr11:102668000-102670800 Enhancers Fetal Intestine Large intestine
16 chr11:102668200-102668600 Active TSS Foreskin Fibroblast Primary Cells skin01 Skin
17 chr11:102668200-102670200 Weak transcription Small Intestine intestine
18 chr11:102668200-102674800 Enhancers NHDF-Ad bronchial

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