Variant report

Variant rs9609598
Chromosome Location chr22:32963998-32963999
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:32953400-32964800 Weak transcription H1 Cell Line embryonic stem cell
2 chr22:32960200-32970600 Weak transcription Lung lung
3 chr22:32960400-32964000 Weak transcription Right Ventricle heart
4 chr22:32960800-32971400 Weak transcription Right Atrium heart
5 chr22:32962200-32964000 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr22:32962200-32964600 Enhancers HepG2 liver
7 chr22:32962800-32965800 Weak transcription K562 blood
8 chr22:32963000-32964400 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
9 chr22:32963400-32964200 Enhancers Fetal Lung lung
10 chr22:32963600-32964000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr22:32963600-32964200 Enhancers Fetal Muscle Trunk muscle
12 chr22:32963600-32964600 Flanking Active TSS Fetal Adrenal Gland Adrenal Gland
13 chr22:32963600-32964800 Enhancers Fetal Muscle Leg muscle
14 chr22:32963800-32964000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr22:32963800-32964000 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr22:32963800-32964200 Enhancers Adipose Nuclei Adipose
17 chr22:32963800-32964200 Enhancers Placenta Placenta
18 chr22:32963800-32965000 Enhancers HUES6 Cell Line embryonic stem cell
19 chr22:32963800-32965000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
20 chr22:32963800-32972200 Weak transcription Spleen Spleen

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