Variant report

Variant rs61366770
Chromosome Location chr2:113869163-113869164
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:113868200-113871400 Weak transcription Gastric stomach
2 chr2:113868400-113869200 Weak transcription Esophagus oesophagus
3 chr2:113868600-113870800 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr2:113868600-113875400 Enhancers Primary monocytes fromperipheralblood blood
5 chr2:113869000-113869400 Enhancers Stomach Mucosa stomach
6 chr2:113869000-113869600 Flanking Active TSS Primary neutrophils fromperipheralblood blood
7 chr2:113869000-113869600 Enhancers Primary B cells from cord blood blood
8 chr2:113869000-113870200 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr2:113869000-113870400 Enhancers Liver Liver
10 chr2:113869000-113870400 Enhancers Placenta Placenta
11 chr2:113869000-113870400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
12 chr2:113869000-113870600 Bivalent Enhancer HepG2 liver

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