Variant report

Variant rs73539228
Chromosome Location chr9:98054954-98054955
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:98046600-98059400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
2 chr9:98046600-98063000 Weak transcription Fetal Stomach stomach
3 chr9:98047200-98059400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
4 chr9:98047400-98055800 Weak transcription HepG2 liver
5 chr9:98048000-98055000 Weak transcription Fetal Intestine Small intestine
6 chr9:98048800-98059200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr9:98050000-98059200 Weak transcription HSMM muscle
8 chr9:98050200-98067400 Weak transcription A549 lung
9 chr9:98051200-98059400 Weak transcription Small Intestine intestine
10 chr9:98054400-98055000 ZNF genes & repeats H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:98054400-98057000 Enhancers Fetal Intestine Large intestine
12 chr9:98054600-98059400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr9:98054800-98055200 ZNF genes & repeats Thymus Thymus
14 chr9:98054800-98055400 Strong transcription Fetal Muscle Leg muscle
15 chr9:98054800-98063000 Weak transcription Lung lung

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