Variant report

Variant rs12112835
Chromosome Location chr7:53664397-53664398
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:53655600-53671400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr7:53662800-53664600 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr7:53663400-53664400 Enhancers NHEK skin
4 chr7:53663400-53664600 Enhancers HMEC breast
5 chr7:53663400-53666800 Enhancers Rectal Smooth Muscle rectum
6 chr7:53663600-53664400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr7:53663600-53664600 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr7:53663600-53664600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr7:53663600-53664600 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr7:53663800-53664600 Enhancers HUVEC blood vessel
11 chr7:53663800-53670400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr7:53664000-53664400 Enhancers HUES64 Cell Line embryonic stem cell
13 chr7:53664200-53665200 Weak transcription Colon Smooth Muscle Colon
14 chr7:53664200-53670400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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