Variant report

Variant rs13006901
Chromosome Location chr2:114586100-114586101
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114574200-114603600 Weak transcription Primary B cells from cord blood blood
2 chr2:114576400-114588400 Weak transcription Esophagus oesophagus
3 chr2:114580400-114588600 Weak transcription K562 blood
4 chr2:114582400-114586800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:114584600-114595600 Weak transcription HepG2 liver
6 chr2:114584800-114592000 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr2:114585400-114586400 Enhancers Fetal Intestine Large intestine
8 chr2:114585600-114586800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr2:114585600-114588400 Weak transcription NHEK skin
10 chr2:114585600-114588600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr2:114585800-114588600 Weak transcription HMEC breast
12 chr2:114585800-114588800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr2:114586000-114586400 Strong transcription Primary T cells from cord blood blood
14 chr2:114586000-114588400 Weak transcription Breast Myoepithelial Primary Cells Breast

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