Variant report

Variant rs9361468
Chromosome Location chr6:79621214-79621215
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:79619200-79621600 Enhancers Fetal Heart heart
2 chr6:79619200-79625800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:79619800-79621400 Flanking Active TSS NHEK skin
4 chr6:79620200-79621400 Flanking Active TSS Duodenum Mucosa Duodenum
5 chr6:79621000-79621400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
6 chr6:79621000-79621800 Weak transcription Fetal Brain Female brain
7 chr6:79621000-79625200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr6:79621200-79621400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr6:79621200-79621600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr6:79621200-79621800 Enhancers NHDF-Ad bronchial
11 chr6:79621200-79622400 Enhancers Fetal Intestine Large intestine
12 chr6:79621200-79622400 Enhancers Fetal Intestine Small intestine
13 chr6:79621200-79625200 Weak transcription Spleen Spleen
14 chr6:79621200-79625200 Weak transcription HMEC breast
15 chr6:79621200-79627800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived

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