Variant report

Variant rs71639168
Chromosome Location chr1:192676690-192676691
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:192671400-192677000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:192671400-192677200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr1:192671600-192676800 Weak transcription Rectal Smooth Muscle rectum
4 chr1:192671800-192677200 Weak transcription NHEK skin
5 chr1:192671800-192678400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr1:192672400-192678000 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr1:192672800-192677800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr1:192673200-192678600 Weak transcription NH-A brain
9 chr1:192674400-192677200 Weak transcription A549 lung
10 chr1:192675200-192676800 Enhancers Primary neutrophils fromperipheralblood blood
11 chr1:192675600-192677600 Enhancers Monocytes-CD14+_RO01746 blood
12 chr1:192676000-192677200 Weak transcription Colon Smooth Muscle Colon
13 chr1:192676400-192677400 Enhancers Primary monocytes fromperipheralblood blood
14 chr1:192676600-192677000 Enhancers Stomach Mucosa stomach
15 chr1:192676600-192677200 Enhancers Primary B cells from cord blood blood
16 chr1:192676600-192677600 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr1:192676600-192679400 Enhancers HepG2 liver

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