Variant report

Variant rs17009886
Chromosome Location chr10:50489950-50489951
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:50485800-50495000 Enhancers Primary monocytes fromperipheralblood blood
2 chr10:50486000-50490400 Enhancers Monocytes-CD14+_RO01746 blood
3 chr10:50487200-50490800 Enhancers Fetal Heart heart
4 chr10:50487400-50490400 Weak transcription K562 blood
5 chr10:50488200-50490400 Weak transcription HSMMtube muscle
6 chr10:50488200-50490600 Weak transcription HSMM muscle
7 chr10:50488200-50490800 Weak transcription Right Atrium heart
8 chr10:50488200-50492400 Weak transcription Lung lung
9 chr10:50488400-50490600 Weak transcription Right Ventricle heart
10 chr10:50488600-50491200 Weak transcription Primary neutrophils fromperipheralblood blood
11 chr10:50488600-50494600 Weak transcription Primary hematopoietic stem cells blood
12 chr10:50488800-50490600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
13 chr10:50489000-50492800 Enhancers Skeletal Muscle Male skeletal muscle
14 chr10:50489200-50490600 Enhancers Skeletal Muscle Female skeletal muscle
15 chr10:50489400-50490000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
16 chr10:50489400-50492000 Enhancers Fetal Muscle Trunk muscle
17 chr10:50489600-50491800 Enhancers Left Ventricle heart
18 chr10:50489600-50491800 Enhancers Psoas Muscle Psoas
19 chr10:50489600-50492800 Enhancers Fetal Muscle Leg muscle

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