Variant report

Variant rs16823157
Chromosome Location chr2:171601801-171601802
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171574000-171620800 Weak transcription Pancreas Pancrea
2 chr2:171597600-171603800 Weak transcription HMEC breast
3 chr2:171597800-171604000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:171598000-171603800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:171600400-171602400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
6 chr2:171600800-171602400 Enhancers Primary neutrophils fromperipheralblood blood
7 chr2:171600800-171604000 Weak transcription iPS-18 Cell Line embryonic stem cell
8 chr2:171601000-171602200 Enhancers Fetal Intestine Small intestine
9 chr2:171601000-171603800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr2:171601200-171602600 Enhancers Primary monocytes fromperipheralblood blood
11 chr2:171601600-171604200 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr2:171601600-171606400 Weak transcription Gastric stomach
13 chr2:171601800-171602000 Enhancers K562 blood
14 chr2:171601800-171604200 Weak transcription Stomach Mucosa stomach

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