Variant report

Variant rs16834675
Chromosome Location chr1:192677326-192677327
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192671800-192678400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
2 chr1:192672400-192678000 Weak transcription ES-I3 Cell Line embryonic stem cell
3 chr1:192672800-192677800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
4 chr1:192673200-192678600 Weak transcription NH-A brain
5 chr1:192675600-192677600 Enhancers Monocytes-CD14+_RO01746 blood
6 chr1:192676400-192677400 Enhancers Primary monocytes fromperipheralblood blood
7 chr1:192676600-192677600 Enhancers Breast Myoepithelial Primary Cells Breast
8 chr1:192676600-192679400 Enhancers HepG2 liver
9 chr1:192676800-192677600 Enhancers Rectal Smooth Muscle rectum
10 chr1:192677000-192677400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:192677000-192682000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
12 chr1:192677200-192677600 Enhancers Colon Smooth Muscle Colon
13 chr1:192677200-192677600 Enhancers NHEK skin
14 chr1:192677200-192679000 Enhancers Primary neutrophils fromperipheralblood blood
15 chr1:192677200-192680000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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