Variant report

Variant rs10119888
Chromosome Location chr9:118613720-118613721
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:25 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:118608400-118617600 Weak transcription iPS-20b Cell Line embryonic stem cell
2 chr9:118610200-118617600 Weak transcription A549 lung
3 chr9:118611200-118613800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
4 chr9:118611200-118613800 Enhancers NHDF-Ad bronchial
5 chr9:118611400-118613800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr9:118611400-118617600 Weak transcription iPS-15b Cell Line embryonic stem cell
7 chr9:118612000-118613800 Enhancers HSMMtube muscle
8 chr9:118612000-118614000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr9:118612200-118613800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
10 chr9:118612200-118613800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr9:118612200-118613800 Enhancers Fetal Stomach stomach
12 chr9:118612200-118613800 Enhancers HMEC breast
13 chr9:118612200-118613800 Enhancers Osteobl bone
14 chr9:118612200-118614200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr9:118612400-118613800 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr9:118612400-118613800 Enhancers NHLF lung
17 chr9:118612800-118613800 Enhancers NHEK skin
18 chr9:118613200-118613800 Enhancers HUES6 Cell Line embryonic stem cell
19 chr9:118613200-118613800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr9:118613200-118613800 Enhancers NH-A brain
21 chr9:118613400-118613800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
22 chr9:118613400-118617400 Weak transcription H9 Cell Line embryonic stem cell
23 chr9:118613400-118617600 Weak transcription ES-I3 Cell Line embryonic stem cell
24 chr9:118613600-118617600 Weak transcription iPS-18 Cell Line embryonic stem cell
25 chr9:118613600-118617800 Weak transcription HSMM muscle

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