Variant report

Variant rs17783271
Chromosome Location chr10:50491364-50491365
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:50485800-50495000 Enhancers Primary monocytes fromperipheralblood blood
2 chr10:50488200-50492400 Weak transcription Lung lung
3 chr10:50488600-50494600 Weak transcription Primary hematopoietic stem cells blood
4 chr10:50489000-50492800 Enhancers Skeletal Muscle Male skeletal muscle
5 chr10:50489400-50492000 Enhancers Fetal Muscle Trunk muscle
6 chr10:50489600-50491800 Enhancers Left Ventricle heart
7 chr10:50489600-50491800 Enhancers Psoas Muscle Psoas
8 chr10:50489600-50492800 Enhancers Fetal Muscle Leg muscle
9 chr10:50490400-50491600 Enhancers K562 blood
10 chr10:50490400-50492000 Enhancers HSMMtube muscle
11 chr10:50490600-50491400 Flanking Active TSS Skeletal Muscle Female skeletal muscle
12 chr10:50490600-50491800 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr10:50490800-50491600 Flanking Active TSS Fetal Heart heart
14 chr10:50490800-50492600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr10:50491000-50492200 Bivalent Enhancer Placenta Placenta
16 chr10:50491000-50493400 Enhancers Monocytes-CD14+_RO01746 blood
17 chr10:50491000-50495800 Weak transcription Spleen Spleen
18 chr10:50491200-50491400 Weak transcription Right Ventricle heart
19 chr10:50491200-50493400 Enhancers Primary neutrophils fromperipheralblood blood
20 chr10:50491200-50496200 Weak transcription Right Atrium heart

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