Variant report

Variant rs10161301
Chromosome Location chr12:44432919-44432920
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44390800-44439200 Weak transcription Esophagus oesophagus
2 chr12:44422200-44437800 Weak transcription Stomach Smooth Muscle stomach
3 chr12:44423200-44434200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr12:44423400-44447000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr12:44429000-44446800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr12:44430200-44440400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
7 chr12:44430400-44439600 Weak transcription Fetal Intestine Large intestine
8 chr12:44431000-44437200 Weak transcription Fetal Stomach stomach
9 chr12:44431400-44446400 Weak transcription Gastric stomach
10 chr12:44431800-44436600 Weak transcription Sigmoid Colon Sigmoid Colon
11 chr12:44432000-44436800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
12 chr12:44432200-44437800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
13 chr12:44432400-44446400 Weak transcription Left Ventricle heart
14 chr12:44432600-44437200 Weak transcription Fetal Intestine Small intestine
15 chr12:44432600-44441000 Weak transcription Breast Myoepithelial Primary Cells Breast

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