Variant report

Variant rs2018140
Chromosome Location chr21:45251207-45251208
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:45211000-45257200 Weak transcription Right Atrium heart
2 chr21:45247000-45255600 Weak transcription Esophagus oesophagus
3 chr21:45250000-45252200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr21:45250600-45256400 Weak transcription K562 blood
5 chr21:45251200-45251400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr21:45251200-45251600 Enhancers Fetal Intestine Small intestine
7 chr21:45251200-45251600 Bivalent Enhancer Fetal Muscle Trunk muscle
8 chr21:45251200-45251600 Enhancers Right Ventricle heart
9 chr21:45251200-45251600 Flanking Bivalent TSS/Enh HepG2 liver
10 chr21:45251200-45254000 Enhancers Monocytes-CD14+_RO01746 blood
11 chr21:45251200-45255000 Enhancers Primary monocytes fromperipheralblood blood

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