Variant report

Variant rs7683968
Chromosome Location chr4:30932371-30932372
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:30914200-30947200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
2 chr4:30914400-30940600 Weak transcription Colon Smooth Muscle Colon
3 chr4:30920600-30947400 Weak transcription Fetal Stomach stomach
4 chr4:30922000-30935800 Weak transcription Aorta Aorta
5 chr4:30922400-30933800 Weak transcription iPS-20b Cell Line embryonic stem cell
6 chr4:30922600-30934200 Weak transcription HUES48 Cell Line embryonic stem cell
7 chr4:30928600-30997400 Weak transcription Fetal Lung lung
8 chr4:30930200-30934200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr4:30930400-30938400 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr4:30931000-30932800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr4:30931000-30934400 Weak transcription HUES64 Cell Line embryonic stem cell
12 chr4:30931800-30934200 Weak transcription iPS-15b Cell Line embryonic stem cell
13 chr4:30932000-30932400 Enhancers Placenta Amnion Placenta Amnion
14 chr4:30932000-30933800 Weak transcription Fetal Intestine Small intestine
15 chr4:30932000-30934000 Weak transcription Fetal Intestine Large intestine
16 chr4:30932000-30935600 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
17 chr4:30932000-30939800 Weak transcription Fetal Heart heart

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