Variant report

Variant rs33945715
Chromosome Location chr1:192673525-192673526
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192669600-192674200 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr1:192670200-192676200 Enhancers HepG2 liver
3 chr1:192671400-192677000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:192671400-192677200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
5 chr1:192671600-192676600 Weak transcription Stomach Mucosa stomach
6 chr1:192671600-192676800 Weak transcription Rectal Smooth Muscle rectum
7 chr1:192671800-192677200 Weak transcription NHEK skin
8 chr1:192671800-192678400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr1:192672000-192675600 Weak transcription Monocytes-CD14+_RO01746 blood
10 chr1:192672200-192675800 Weak transcription Primary monocytes fromperipheralblood blood
11 chr1:192672400-192675600 Weak transcription Colon Smooth Muscle Colon
12 chr1:192672400-192678000 Weak transcription ES-I3 Cell Line embryonic stem cell
13 chr1:192672800-192677800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr1:192673200-192674200 Weak transcription A549 lung
15 chr1:192673200-192674400 Weak transcription HMEC breast
16 chr1:192673200-192678600 Weak transcription NH-A brain
17 chr1:192673400-192673600 Enhancers Primary neutrophils fromperipheralblood blood
18 chr1:192673400-192673600 Flanking Active TSS GM12878-XiMat blood

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