Variant report

Variant rs12278712
Chromosome Location chr11:15515767-15515768
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:15512200-15520400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr11:15514600-15523200 Enhancers Fetal Intestine Large intestine
3 chr11:15514800-15516200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
4 chr11:15514800-15516600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
5 chr11:15514800-15520200 Enhancers Liver Liver
6 chr11:15514800-15522400 Enhancers Fetal Intestine Small intestine
7 chr11:15515200-15515800 Enhancers Placenta Placenta
8 chr11:15515200-15516200 Enhancers Rectal Mucosa Donor 31 rectum
9 chr11:15515400-15515800 Enhancers Psoas Muscle Psoas
10 chr11:15515400-15516000 Enhancers Fetal Muscle Leg muscle
11 chr11:15515400-15516000 Enhancers Stomach Mucosa stomach
12 chr11:15515400-15516000 Enhancers HSMM muscle
13 chr11:15515400-15516200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
14 chr11:15515400-15516600 Enhancers Pancreas Pancrea
15 chr11:15515600-15515800 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
16 chr11:15515600-15516000 Enhancers Fetal Kidney kidney
17 chr11:15515600-15516000 Enhancers Fetal Lung lung

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