Variant report

Variant rs7683379
Chromosome Location chr4:1045824-1045825
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1038600-1046000 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr4:1040800-1048600 Weak transcription Right Atrium heart
3 chr4:1041200-1049200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr4:1042000-1046200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
5 chr4:1042200-1052200 Weak transcription Gastric stomach
6 chr4:1044800-1046000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr4:1044800-1046000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
8 chr4:1044800-1047800 Bivalent Enhancer Fetal Muscle Leg muscle
9 chr4:1045000-1046600 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
10 chr4:1045600-1046800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr4:1045800-1046400 Enhancers Breast Myoepithelial Primary Cells Breast
12 chr4:1045800-1046400 ZNF genes & repeats Spleen Spleen
13 chr4:1045800-1046600 Bivalent Enhancer Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:1045800-1046600 Bivalent Enhancer Osteobl bone
15 chr4:1045800-1046800 Bivalent Enhancer Muscle Satellite Cultured Cells --
16 chr4:1045800-1046800 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
17 chr4:1045800-1047200 Bivalent Enhancer Fetal Muscle Trunk muscle
18 chr4:1045800-1047600 Bivalent Enhancer NHDF-Ad bronchial

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