Variant report

Variant rs71604339
Chromosome Location chr4:1047970-1047971
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1040800-1048600 Weak transcription Right Atrium heart
2 chr4:1041200-1049200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
3 chr4:1042200-1052200 Weak transcription Gastric stomach
4 chr4:1046600-1049200 Weak transcription Lung lung
5 chr4:1047000-1049200 Active TSS Right Ventricle heart
6 chr4:1047200-1049200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr4:1047200-1049200 Weak transcription Spleen Spleen
8 chr4:1047400-1049800 Bivalent Enhancer Fetal Muscle Trunk muscle
9 chr4:1047600-1048000 Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr4:1047600-1048000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr4:1047600-1048000 Active TSS Psoas Muscle Psoas
12 chr4:1047600-1048000 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
13 chr4:1047600-1049400 Active TSS Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr4:1047800-1048000 Flanking Bivalent TSS/Enh Breast Myoepithelial Primary Cells Breast
15 chr4:1047800-1048000 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
16 chr4:1047800-1048000 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle

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