Variant report

Variant rs7039117
Chromosome Location chr9:98057180-98057181
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 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 chr9:98048800-98059200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr9:98050000-98059200 Weak transcription HSMM muscle
6 chr9:98050200-98067400 Weak transcription A549 lung
7 chr9:98051200-98059400 Weak transcription Small Intestine intestine
8 chr9:98054600-98059400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr9:98054800-98063000 Weak transcription Lung lung
10 chr9:98055000-98068600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
11 chr9:98055200-98065600 Weak transcription Thymus Thymus
12 chr9:98055400-98066000 Weak transcription Fetal Muscle Leg muscle
13 chr9:98055600-98062000 Weak transcription Aorta Aorta
14 chr9:98056200-98059600 Weak transcription Fetal Intestine Small intestine
15 chr9:98057000-98059000 Weak transcription HepG2 liver
16 chr9:98057000-98059400 Weak transcription Fetal Intestine Large intestine
17 chr9:98057000-98059400 Weak transcription Sigmoid Colon Sigmoid Colon

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