Variant report

Variant rs12074592
Chromosome Location chr1:69592299-69592300
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:69586400-69592400 Weak transcription iPS-15b Cell Line embryonic stem cell
2 chr1:69586400-69596800 Weak transcription HUES48 Cell Line embryonic stem cell
3 chr1:69586800-69592400 Weak transcription H1 Cell Line embryonic stem cell
4 chr1:69588000-69592400 Weak transcription NHEK skin
5 chr1:69588800-69592400 Weak transcription Aorta Aorta
6 chr1:69588800-69593600 Weak transcription Colon Smooth Muscle Colon
7 chr1:69589000-69593400 Weak transcription Stomach Smooth Muscle stomach
8 chr1:69592000-69592400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr1:69592000-69593000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
10 chr1:69592000-69593000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:69592000-69594800 Enhancers Fetal Brain Male brain
12 chr1:69592200-69592400 Enhancers Fetal Brain Female brain
13 chr1:69592200-69593600 Enhancers Fetal Adrenal Gland Adrenal Gland

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