Variant report

Variant rs7027785
Chromosome Location chr9:93824836-93824837
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93821800-93826200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr9:93822000-93825800 Enhancers Skeletal Muscle Female skeletal muscle
3 chr9:93822000-93826400 Enhancers Skeletal Muscle Male skeletal muscle
4 chr9:93823000-93826200 Enhancers Psoas Muscle Psoas
5 chr9:93823400-93825200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr9:93823600-93825400 Enhancers HepG2 liver
7 chr9:93824000-93825400 Enhancers Hela-S3 cervix
8 chr9:93824000-93833400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr9:93824400-93825000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr9:93824400-93825200 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
11 chr9:93824400-93825200 Enhancers Lung lung
12 chr9:93824400-93825800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
13 chr9:93824600-93833400 Weak transcription NHLF lung
14 chr9:93824800-93825000 Enhancers Liver Liver
15 chr9:93824800-93827600 Weak transcription Esophagus oesophagus
16 chr9:93824800-93833400 Weak transcription Spleen Spleen

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