| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18948 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr21:37560230-37561120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr21:37560535-37560551 | CCTTGTTTACATAGGA | - | 6.35 | | Foxa2 | MA0047.2 | chr21:37560538-37560550 | TGTTTACATAGG | + | 6.92 | | INSM1 | MA0155.1 | chr21:37560817-37560829 | TGCCCCCTGGCA | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 37560400 | 37560800 | | chr21 | 37560853 | 37561049 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I036186 | chr21 | 37558989 | 37561608 |
|
Enhancer Sequence | TCTCTAGTAG GTGATACACC CAGCCTTCAG TTCTACTCCT ACTCAAGCAG CATGGTAATT 60
TTAAGAAAAT TTTAAAAGGA AAAAAAAAGC ATATTCTAAT GTGTCTTCTT ACCTGATGCA 120
GAAGATGGAG TTAGCCTGAG TGACCCATTC CTTGCTAGCA GCTTTATTGG AAGCTGGGAT 180
TTGGGTATGT GGATAACTCA TGCTGAGAGC TGATTAATCA CGTGCATGGC CCTGTTAGGG 240
TTCAACTGAC TTAGGTAAAT ACAACACAAT GATATTTCAG CTGTGACCTT TCAGAGAAGG 300
AAGCTCCTTG TTTACATAGG AGTTATAGCA GCACTGCTCT CCCAGTTCAA CAAAAACTGG 360
TCTCACTGGT TACCTGTGGA ACCCCGACTC CCTGAGATGG CTCTCGGCAG CCTTGCCTTC 420
TGCCTGTTTC TCCAGCTTAT CTCTTGCCAC CGCCACTCCC TCAAGCTGGC AAAGCAACCG 480
GGTCATGCCA TTTCAGTCAA GGTGGAATGC CACACCATGA GCACTTGGGA AGTCCTGGCC 540
AAGTGCTGGT CTGTTCCATT TTCGTCCTGT CTAAAGGGCA CTAACAGTGC CCCCTGGCAG 600
GTGCTTCACT GAGCGTTTGA GCCTGTGTCA CCTGGCCTCC CTGACTCACT GTGCCACTGT 660
GCAGCTTCCT TTCAGTGGCA TGAAAAGAAC ACCCTTACAA AGATGCCTGA CTTCCAGAAG 720
GAAGACATGT CAGTGTTTCA CCGTGAAAAA TGCAACTCCT CGTTTGCTTG GTGGGAGACG 780
TGCTTTTAAA TTGGCTGACT TACATTTCTT TCTAGACAAA GACATCTGGC ATTCTGAAGT 840
CAGCATTGTA CTCTGTGCAA AAGTAGGGTG ACTGTCTCTT CTAGGAACTT 890
|
