Variant report

Variant rs72948697
Chromosome Location chr2:114591972-114591973
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114574200-114603600 Weak transcription Primary B cells from cord blood blood
2 chr2:114584600-114595600 Weak transcription HepG2 liver
3 chr2:114584800-114592000 Weak transcription ES-I3 Cell Line embryonic stem cell
4 chr2:114586400-114601000 Weak transcription Primary T cells from cord blood blood
5 chr2:114589200-114592000 Weak transcription HMEC breast
6 chr2:114589200-114596400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
7 chr2:114589200-114600200 Weak transcription Breast Myoepithelial Primary Cells Breast
8 chr2:114589200-114600200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:114589200-114600200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr2:114591200-114592800 Enhancers Placenta Placenta
11 chr2:114591400-114592000 Enhancers Fetal Intestine Large intestine
12 chr2:114591400-114592600 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr2:114591600-114592400 Flanking Active TSS Primary neutrophils fromperipheralblood blood
14 chr2:114591600-114592600 Enhancers Monocytes-CD14+_RO01746 blood
15 chr2:114591600-114597800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
16 chr2:114591800-114592800 Enhancers Primary monocytes fromperipheralblood blood

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