Variant report

Variant rs2073962
Chromosome Location chr7:18833355-18833356
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:18790600-18835000 Weak transcription Primary B cells from cord blood blood
2 chr7:18832200-18833400 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
3 chr7:18832400-18833600 Enhancers Fetal Stomach stomach
4 chr7:18832400-18834200 Active TSS Aorta Aorta
5 chr7:18832600-18833400 Flanking Active TSS Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr7:18832600-18833800 Enhancers HUES48 Cell Line embryonic stem cell
7 chr7:18832800-18833400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
8 chr7:18832800-18833400 Active TSS Duodenum Smooth Muscle Duodenum
9 chr7:18833000-18833400 Flanking Active TSS Colon Smooth Muscle Colon
10 chr7:18833000-18833400 Enhancers Rectal Smooth Muscle rectum
11 chr7:18833000-18833600 Flanking Active TSS Stomach Smooth Muscle stomach
12 chr7:18833000-18837200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
13 chr7:18833000-18837800 Weak transcription HUES6 Cell Line embryonic stem cell
14 chr7:18833200-18833400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
15 chr7:18833200-18833400 Enhancers Osteobl bone
16 chr7:18833200-18837800 Weak transcription NH-A brain
17 chr7:18833200-18838000 Weak transcription H1 Cell Line embryonic stem cell

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