Variant report

Variant rs72948681
Chromosome Location chr2:114581489-114581490
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114568200-114586000 Weak transcription Primary T cells from cord blood blood
2 chr2:114574200-114603600 Weak transcription Primary B cells from cord blood blood
3 chr2:114576400-114582800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
4 chr2:114576400-114588400 Weak transcription Esophagus oesophagus
5 chr2:114577000-114583800 Weak transcription HUES64 Cell Line embryonic stem cell
6 chr2:114577200-114582200 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr2:114577200-114584600 Weak transcription Fetal Intestine Small intestine
8 chr2:114578200-114582200 Weak transcription Breast Myoepithelial Primary Cells Breast
9 chr2:114580400-114583800 Weak transcription iPS-18 Cell Line embryonic stem cell
10 chr2:114580400-114588600 Weak transcription K562 blood
11 chr2:114580800-114581800 Flanking Active TSS Foreskin Melanocyte Primary Cells skin03 Skin
12 chr2:114581000-114582400 Enhancers NHDF-Ad bronchial
13 chr2:114581400-114582400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr2:114581400-114583200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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