Variant report

Variant rs1078139
Chromosome Location chr4:828148-828149
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:821000-828800 Weak transcription Right Atrium heart
2 chr4:825600-829000 Weak transcription Left Ventricle heart
3 chr4:825600-829000 Weak transcription Right Ventricle heart
4 chr4:825600-831600 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
5 chr4:826400-829200 Bivalent Enhancer Placenta Placenta
6 chr4:826400-829600 Enhancers Primary Natural Killer cells fromperipheralblood blood
7 chr4:826400-830600 Weak transcription Brain Germinal Matrix brain
8 chr4:826600-828200 Bivalent Enhancer Primary T cells fromperipheralblood blood
9 chr4:826600-829600 Bivalent Enhancer Fetal Muscle Trunk muscle
10 chr4:826800-828400 Weak transcription Spleen Spleen
11 chr4:826800-828800 Enhancers HSMMtube muscle
12 chr4:827000-828200 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
13 chr4:827200-831600 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr4:827400-828600 Enhancers HSMM muscle
15 chr4:827600-829000 Weak transcription Esophagus oesophagus
16 chr4:827800-830200 Bivalent/Poised TSS Foreskin Fibroblast Primary Cells skin02 Skin
17 chr4:828000-828200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr4:828000-828200 Bivalent Enhancer Skeletal Muscle Male skeletal muscle

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