Variant report

Variant rs556445072
Chromosome Location chr2:112285272-112285273
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:112270800-112286200 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
2 chr2:112277600-112292600 Weak transcription Placenta Amnion Placenta Amnion
3 chr2:112280800-112291600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
4 chr2:112280800-112292600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr2:112281000-112290200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
6 chr2:112281000-112291400 Weak transcription K562 blood
7 chr2:112281000-112291600 Weak transcription Right Ventricle heart
8 chr2:112282200-112288000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
9 chr2:112282400-112289200 Weak transcription NHLF lung
10 chr2:112282400-112291600 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr2:112282400-112291600 Weak transcription H1 Cell Line embryonic stem cell
12 chr2:112282600-112291600 Weak transcription H9 Cell Line embryonic stem cell
13 chr2:112282600-112292400 Weak transcription iPS-20b Cell Line embryonic stem cell
14 chr2:112282800-112288800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
15 chr2:112284000-112285600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
16 chr2:112284600-112288000 Weak transcription Primary monocytes fromperipheralblood blood
17 chr2:112284600-112289000 Weak transcription Monocytes-CD14+_RO01746 blood
18 chr2:112285200-112285400 Enhancers NHDF-Ad bronchial
19 chr2:112285200-112286200 Enhancers HepG2 liver

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