Variant report

Variant rs17029269
Chromosome Location chr4:100575398-100575399
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:100566600-100575800 Weak transcription Fetal Heart heart
2 chr4:100567800-100579200 Weak transcription Stomach Smooth Muscle stomach
3 chr4:100570200-100575600 Weak transcription Left Ventricle heart
4 chr4:100570200-100576200 Weak transcription Fetal Lung lung
5 chr4:100570800-100575400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr4:100571000-100576000 Active TSS Psoas Muscle Psoas
7 chr4:100571000-100576200 Weak transcription Brain Anterior Caudate brain
8 chr4:100572000-100575800 Flanking Active TSS Fetal Muscle Trunk muscle
9 chr4:100573400-100575400 Active TSS Skeletal Muscle Female skeletal muscle
10 chr4:100574200-100576000 Enhancers Ovary ovary
11 chr4:100574400-100575800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
12 chr4:100574600-100575400 Active TSS Right Ventricle heart
13 chr4:100574600-100575600 Flanking Active TSS Fetal Muscle Leg muscle
14 chr4:100574800-100576200 Active TSS Skeletal Muscle Male skeletal muscle
15 chr4:100575000-100575400 Flanking Bivalent TSS/Enh Muscle Satellite Cultured Cells --
16 chr4:100575000-100576000 Flanking Active TSS HSMMtube muscle
17 chr4:100575000-100577200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
18 chr4:100575200-100575800 Enhancers Right Atrium heart
19 chr4:100575200-100576000 Flanking Active TSS HSMM muscle
20 chr4:100575200-100577200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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