| Tag | Content |
|---|
EnhancerAtlas ID | HS037-09593 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr12:121417950-121418850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr12:121418141-121418162 | TTTTCTGTCCAAGGTCCTGAT | - | 7.18 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23495 | chr12:121415641-121419989 | Colon_Crypt_1 | | SE_24673 | chr12:121415750-121418798 | Colon_Crypt_2 | | SE_27808 | chr12:121415253-121422996 | Fetal_Intestine | | SE_28751 | chr12:121414723-121423182 | Fetal_Intestine_Large | | SE_32255 | chr12:121415237-121423194 | Gastric | | SE_53251 | chr12:121415308-121420038 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCTGCTTCAC AAATGGGGAA ACTGGGGCTT AGAGCCGGGA AGGAGCTAGA CTAAGTTCAC 60
CAAACTGAGG CCCCAAACCT ACTCTGTTCG GTGCTCTCAA TTGCTATGAC CGGGGACCAG 120
AGGCCTGCAG GGGGTGGCCA GGGAGTCAGA GAGAGACCGA GCCCCAAAGA TGCTCCAAAG 180
GGGCCCATCT CTTTTCTGTC CAAGGTCCTG ATCCCAGCTG GGGTGGGGGA GGGCTGGTGG 240
ATTCCTGCTT TCCCAGAGGC CTCAGGGAGC CTCCCGAGGG CCTGGACAGG GGGCAGGGGA 300
GCAGTCAGGG CCCCCTGACT TGGCAGGAAG AGGAGGGCAA AGGACTCCAG AGCTGCAGGG 360
GAGGGGCAAA GAGTCAGGCA TCCCAGACCC AGGGCGAAGG CAACCTGACG GGGTGGGGCT 420
GGGCCTGACC TGCCCAGGGC CCCAGATGGG ACTGGGGGCT TTGGGGTGAG GGTGGGGGCA 480
GGGGATGCTT TCTTACCTGG CTGAGTGAGC TCTCTCGGTC AGCAGCCCCC TTTGGTGGGA 540
TGGTGGGGTT GGGGAGGCTT GATCCACAGC ATTTGAAGGG GAAGCAGAGG TCAAAGTGCT 600
TCCTAGGGAC CAGCAGAGAC CTGGAAGCTG AGGCAGAGAG TGTAGAGAGA GGCCATTGGG 660
GGAGATGGAC AGAGAAGCTG GGAGAAGCAG AACGGAGGAG CCAGGGGGGC GGGGGCTCAG 720
ACCCAGCTGG GAGAAGGGGC ACGGGAGAGA ATGAGGCGCC CCAAGCTTGC AAGGAGGCTG 780
GAGTGCTTCC CGCCTGCCCC GATTGGGTTT TCTTTAATGC TAACAGCATG CTATTTACTT 840
TCCATTTAAA TTTGAGATGT TGCTATAAAT TATCAACCAG CTCCTTGTTC CTGCAGAGTT 900
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