Variant report

Variant rs73034169
Chromosome Location chr1:173090361-173090362
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:173081600-173091200 Weak transcription NHDF-Ad bronchial
2 chr1:173082400-173091200 Weak transcription NHLF lung
3 chr1:173082800-173091000 Weak transcription HSMM muscle
4 chr1:173084400-173091000 Weak transcription Fetal Intestine Large intestine
5 chr1:173086600-173091400 Weak transcription Fetal Heart heart
6 chr1:173086600-173091800 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr1:173087000-173091000 Weak transcription Fetal Lung lung
8 chr1:173087000-173091000 Weak transcription HUVEC blood vessel
9 chr1:173087600-173091000 Weak transcription Primary monocytes fromperipheralblood blood
10 chr1:173087600-173091200 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr1:173087600-173092600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
12 chr1:173088800-173091800 Weak transcription Primary B cells from peripheral blood blood
13 chr1:173089000-173091600 Weak transcription Primary B cells from cord blood blood
14 chr1:173089600-173090400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chr1:173089800-173090600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
16 chr1:173089800-173091800 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr1:173090000-173091800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung

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