Variant report

Variant rs12619451
Chromosome Location chr2:112286267-112286268
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:112277600-112292600 Weak transcription Placenta Amnion Placenta Amnion
2 chr2:112280800-112291600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr2:112280800-112292600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr2:112281000-112290200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr2:112281000-112291400 Weak transcription K562 blood
6 chr2:112281000-112291600 Weak transcription Right Ventricle heart
7 chr2:112282200-112288000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr2:112282400-112289200 Weak transcription NHLF lung
9 chr2:112282400-112291600 Weak transcription ES-I3 Cell Line embryonic stem cell
10 chr2:112282400-112291600 Weak transcription H1 Cell Line embryonic stem cell
11 chr2:112282600-112291600 Weak transcription H9 Cell Line embryonic stem cell
12 chr2:112282600-112292400 Weak transcription iPS-20b Cell Line embryonic stem cell
13 chr2:112282800-112288800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr2:112284600-112288000 Weak transcription Primary monocytes fromperipheralblood blood
15 chr2:112284600-112289000 Weak transcription Monocytes-CD14+_RO01746 blood
16 chr2:112285600-112286400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
17 chr2:112285600-112286400 Enhancers HSMM muscle
18 chr2:112285600-112288600 Enhancers Primary T helper 17 cells PMA-I stimulated --
19 chr2:112285800-112286400 Enhancers NHDF-Ad bronchial
20 chr2:112286200-112286400 Flanking Active TSS HepG2 liver
21 chr2:112286200-112286800 Enhancers Fetal Intestine Large intestine
22 chr2:112286200-112287600 Enhancers H9 Derived Neuron Cultured Cells ES cell derived

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