Variant report

Variant rs71522456
Chromosome Location chr1:192675993-192675994
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192670200-192676200 Enhancers HepG2 liver
2 chr1:192671400-192677000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:192671400-192677200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:192671600-192676600 Weak transcription Stomach Mucosa stomach
5 chr1:192671600-192676800 Weak transcription Rectal Smooth Muscle rectum
6 chr1:192671800-192677200 Weak transcription NHEK skin
7 chr1:192671800-192678400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr1:192672400-192678000 Weak transcription ES-I3 Cell Line embryonic stem cell
9 chr1:192672800-192677800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
10 chr1:192673200-192678600 Weak transcription NH-A brain
11 chr1:192674400-192677200 Weak transcription A549 lung
12 chr1:192674800-192676600 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr1:192675200-192676800 Enhancers Primary neutrophils fromperipheralblood blood
14 chr1:192675600-192676000 Enhancers Colon Smooth Muscle Colon
15 chr1:192675600-192677600 Enhancers Monocytes-CD14+_RO01746 blood
16 chr1:192675800-192676000 Enhancers Primary monocytes fromperipheralblood blood
17 chr1:192675800-192676000 Enhancers Primary B cells from cord blood blood

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