Variant report

Variant rs59581968
Chromosome Location chr9:93943140-93943141
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93932200-93944000 Weak transcription K562 blood
2 chr9:93939400-93943400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr9:93939800-93943200 Enhancers Placenta Amnion Placenta Amnion
4 chr9:93940000-93944600 Weak transcription HepG2 liver
5 chr9:93940400-93949000 Weak transcription Spleen Spleen
6 chr9:93940800-93946000 Weak transcription Stomach Mucosa stomach
7 chr9:93940800-93954000 Weak transcription Sigmoid Colon Sigmoid Colon
8 chr9:93941000-93944400 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr9:93941000-93944800 Weak transcription Primary B cells from peripheral blood blood
10 chr9:93941000-93953400 Weak transcription Skeletal Muscle Female skeletal muscle
11 chr9:93941000-93957400 Weak transcription Gastric stomach
12 chr9:93942000-93944400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
13 chr9:93942200-93950000 Weak transcription HSMM muscle
14 chr9:93942400-93943400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr9:93942400-93950000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr9:93942600-93943200 Genic enhancers Foreskin Fibroblast Primary Cells skin01 Skin
17 chr9:93942600-93943200 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr9:93942600-93944000 Weak transcription Esophagus oesophagus
19 chr9:93942800-93943600 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
20 chr9:93942800-93944000 Weak transcription HMEC breast
21 chr9:93942800-93948600 Weak transcription Right Ventricle heart
22 chr9:93942800-93948600 Weak transcription NHLF lung
23 chr9:93942800-93949000 Weak transcription NHDF-Ad bronchial
24 chr9:93943000-93943200 Enhancers iPS DF 19.11 Cell Line embryonic stem cell

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