| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08839 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:131232380-131233140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:131232857-131232876 | TGGCGCCACCTACTGACAG | - | 6.27 | | NFIC | MA0161.2 | chr12:131232486-131232497 | TTCTTGGCAGA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I130748 | chr12 | 131232761 | 131232930 |
|
Enhancer Sequence | GCTATTTTCA CTCCTGCTCC CTCCATAGGA AAGGGTTTAG ACCAACAGGG TCAGCTCTCC 60
ACTCTCCCAG CCTCTCTGTC CCCTCAGAGG AAAAAGCTGC ATAAGCTTCT TGGCAGAACT 120
CTCCACTGTT TCTCTCTCCA CCGACAGCTT CTCCGCCCCT TGCATTTTCC TGTTTTCACT 180
TTGCTTCACA ACCGCCTGAG ATTATCTGAT TTTTAAGGGC AGCACTTGGC TCTGGCTGTG 240
CTTTATAGAG CCCAAGGTGT GCTTAGGTGC CCTCGATGGT AGTAATTTGT CACTGTCTAG 300
CTTGGCATGC CCCCTGCTCC ATGCAGGCCT CCAGCCACAG GGGAGCCAGG CCCCACACAC 360
ATGCAGAAAT TGCAAAATCA CCAGTTGCAC ATGGGATGGC AGAGAACCAG GGGCTTCACT 420
TTAAGGCCAG GCTGGCTCGC ACCAGCCCTG ACGCAGCCTG AGACAACTGC CACCCTCTGG 480
CGCCACCTAC TGACAGCTTT CCCTCTCCCT CGAAGCCTCT GCACCCGCAA TAAAAAAGGG 540
AAGCGTTTGA GCTGACTGCA GCCTCTTCTG TAACTACCAC TATGAGAATG GAAGGATAGC 600
ATTCAGATGC CTAAGGTAAT ACAGTAATGC ATGCCCCTTG CAGAAGACAC AAAAAAGCCC 660
AAAGCAAAAT GTCAAGTCCA CCCCAAAAAG CCCTTCTTTG AAATAACCGT TGCTGGTATT 720
TTTGGGACCT ACCTTTCCAA TGTATTTTAT GTTATTATTT 760
|
