Variant report

Variant rs3996259
Chromosome Location chr9:96572669-96572670
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:96571400-96576000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr9:96571600-96574200 Enhancers K562 blood
3 chr9:96572000-96572800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
4 chr9:96572000-96573200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
5 chr9:96572000-96574200 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr9:96572000-96574200 Bivalent Enhancer Fetal Stomach stomach
7 chr9:96572200-96572800 Enhancers HUES64 Cell Line embryonic stem cell
8 chr9:96572200-96573000 Enhancers Placenta Amnion Placenta Amnion
9 chr9:96572200-96573200 Enhancers ES-WA7 Cell Line embryonic stem cell
10 chr9:96572200-96573800 Enhancers H1 Cell Line embryonic stem cell
11 chr9:96572200-96574400 Enhancers HUES6 Cell Line embryonic stem cell
12 chr9:96572400-96572800 Enhancers Stomach Smooth Muscle stomach
13 chr9:96572400-96573200 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
14 chr9:96572400-96573400 Enhancers Fetal Lung lung
15 chr9:96572400-96573600 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
16 chr9:96572600-96572800 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
17 chr9:96572600-96572800 Flanking Bivalent TSS/Enh Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr9:96572600-96572800 Bivalent Enhancer Fetal Intestine Small intestine
19 chr9:96572600-96572800 Flanking Bivalent TSS/Enh Fetal Muscle Leg muscle
20 chr9:96572600-96573000 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle
21 chr9:96572600-96573200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
22 chr9:96572600-96576400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell

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