Variant report

Variant rs12134818
Chromosome Location chr1:172431435-172431436
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:172422600-172435400 Weak transcription Placenta Amnion Placenta Amnion
2 chr1:172423400-172434600 Weak transcription HSMMtube muscle
3 chr1:172423600-172432000 Weak transcription Primary neutrophils fromperipheralblood blood
4 chr1:172425800-172435400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:172426000-172436000 Weak transcription Fetal Intestine Large intestine
6 chr1:172426400-172434600 Weak transcription Fetal Muscle Leg muscle
7 chr1:172429800-172431600 Enhancers A549 lung
8 chr1:172430200-172435400 Weak transcription HepG2 liver
9 chr1:172430400-172431600 Enhancers Pancreatic Islets Pancreatic Islet
10 chr1:172430400-172435200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:172430400-172435400 Weak transcription HMEC breast
12 chr1:172430600-172435200 Weak transcription NHEK skin
13 chr1:172430600-172436000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
14 chr1:172431200-172435000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
15 chr1:172431200-172435400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
16 chr1:172431400-172431600 Enhancers iPS-20b Cell Line embryonic stem cell

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