Variant report

Variant rs10965037
Chromosome Location chr9:21496372-21496373
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:21463000-21502200 Weak transcription HSMM muscle
2 chr9:21466000-21527600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr9:21471600-21505600 Weak transcription HUVEC blood vessel
4 chr9:21477000-21505800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
5 chr9:21479600-21505000 Weak transcription NHLF lung
6 chr9:21481800-21500000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr9:21481800-21504800 Weak transcription NHDF-Ad bronchial
8 chr9:21481800-21505000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr9:21482000-21504800 Weak transcription NHEK skin
10 chr9:21483200-21501200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr9:21483200-21502200 Weak transcription Muscle Satellite Cultured Cells --
12 chr9:21483200-21504800 Weak transcription HMEC breast
13 chr9:21486000-21498600 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr9:21486000-21499000 Weak transcription A549 lung
15 chr9:21487200-21500600 Weak transcription Osteobl bone
16 chr9:21494200-21503600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr9:21494400-21499400 Weak transcription Fetal Intestine Small intestine
18 chr9:21494800-21527600 Weak transcription Gastric stomach
19 chr9:21495200-21497400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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