The 2.0 version of rSNPBase

Variant report

Variant rs12301421
Chromosome Location chr12:44346015-44346016
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:44324800-44352600 Weak transcription Left Ventricle heart
2 chr12:44326600-44347800 Weak transcription Breast Myoepithelial Primary Cells Breast
3 chr12:44332200-44353200 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr12:44340000-44349600 Weak transcription Fetal Kidney kidney
5 chr12:44341200-44349200 Weak transcription Adipose Nuclei Adipose
6 chr12:44341800-44346200 Strong transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr12:44342000-44347000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr12:44342000-44367200 Weak transcription Sigmoid Colon Sigmoid Colon
9 chr12:44342200-44347400 Weak transcription Gastric stomach
10 chr12:44343400-44347000 Weak transcription Fetal Intestine Large intestine
11 chr12:44343400-44347200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr12:44343600-44359400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr12:44343600-44363400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr12:44343600-44376800 Weak transcription Pancreas Pancrea
15 chr12:44344400-44347200 Weak transcription Stomach Smooth Muscle stomach
16 chr12:44345600-44349800 Weak transcription Aorta Aorta
17 chr12:44346000-44357800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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Last update: Aug 31, 2015