Variant report

Variant rs71639169
Chromosome Location chr1:192678226-192678227
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 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 chr1:192673200-192678600 Weak transcription NH-A brain
3 chr1:192676600-192679400 Enhancers HepG2 liver
4 chr1:192677000-192682000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr1:192677200-192679000 Enhancers Primary neutrophils fromperipheralblood blood
6 chr1:192677200-192680000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:192677400-192680000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
8 chr1:192677400-192683000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr1:192677600-192678600 Weak transcription Breast Myoepithelial Primary Cells Breast
10 chr1:192677600-192678800 Weak transcription NHEK skin
11 chr1:192677800-192682800 Weak transcription HMEC breast
12 chr1:192678000-192678400 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
13 chr1:192678200-192680200 Enhancers Cortex derived primary cultured neurospheres brain
14 chr1:192678200-192681000 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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