| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00247 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:17754140-17755560 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr1:17755015-17755026 | AAGCCATAAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_68792 | chr1:17753490-17755305 | H9 | | SE_68792 | chr1:17755395-17756576 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I017426 | chr1 | 17753491 | 17755305 | | GH01I017429 | chr1 | 17755521 | 17755670 |
|
Enhancer Sequence | GCAAGGGTGC GGTGCCACAC TTGAACTTGC TTGGCCAAGG GGAGTCTCAG GTGGTCAGAT 60
GCTCCTGGAC TTACCAAAGC ATCTTTCCCT GCAGTGCCCA GGATGCCACT GGCTCCTGAG 120
GAGCCGGGTT GGGTTTCTTC CGGCCTCCCA AGGAAGGGCT GGAGGGACTG GAGGGACCGG 180
GCAGGGGTGG GGGAGGGGGA GCAAGTCAAA TTAAACGCCC TGCAGCAGTC CCAGGCTCTG 240
CGGTCAGACT GAGAAGTCAA TTCCCACGGC CTCCGGATCC CTGGGGTCTG GTCCCAATCA 300
CAGAGCTACT GTGTGGCTTG CTGTGGTGCT ATCTTGCAAA AACCAAGACA TCCAGGCTGC 360
TGGTTTTCAC CAGATCTACA GCAACATACA TGCGCGGGAG GCAACAGAGT TAACTAGAGA 420
GTGGGACTCC AACCCTGGCC CTGCCACTCG CTTCCTTTGG TATTTACTGC CCTTCCCTGG 480
GCTTCTGTAT CTTCAATGTC AACTGGGCTG CTCAGTTGAA GAACGGCTTT GAGAAATGAT 540
GCAACACGGG CACAGGACTG GCAACAAGGC GCCATCAGCA CCTGGGCTTA CGTTACTGTA 600
GACCAGGAGG TGCTTCCCTG GGACAAAAGC CACCATGTGG ACGTGGCCCC CTCTGGCTTG 660
GGCCTGAAGG CTGGGCATTT TCCAAACAAC GCGCTGCTGC TACCTGCAAC TTAAACCCAT 720
TTCTAATTCA GCTGGCCCCC AGGTGTTTTC ATGGAACAAG GTGATTTCCA ACGCCCCTGT 780
TTTAAGGTGC CAAGACGAGC CAGCGTGCAA ATATTTGTTC ATGGGGCAAA GCAATGCTGG 840
AAAGCACTTT GGGAGTCTTT CCAGATGAAA TCAAGAAGCC ATAAAAGTTG GCTACATGCC 900
AGCCTTCCTT CTCCTGGATG GGCCTTTTCC CTTAAGACAC CAGTTTTCCA AAGGTAACTG 960
GGGACAAAAC ATTACTTCTT AAGGACCTCT CTGCTTTCCC CCGCTCCAGA CTGTTCTGTC 1020
AAACCAGTTC CTGCAACAAT TTGGCAGCTT GCAAAGAAAC GTGGACTCTT CTGCAATGCC 1080
TGAAATTTTG ACACCTGACA TTTGACAAAT GTCTAGGACA TTCTGACACC ATCTCACAGA 1140
CCTGGTCTCT TCATTTTAAT GAAAACAAGT GAGGTGAGAG GGAAGATGGA AAAGGTGGCA 1200
ATGTTCATTT GAGGATACTA CTTGTATTTT CCTGATTAAT CTTAACGGAA TTAGTGAGTC 1260
ACTTCAAAAT TGTGCCTTTA AAAGACTAAG ATTAGGGTTC AAATCCAGCT CATCACTACA 1320
GTGGCTGTGT GGCCTCAGGC AAGTCACTTG GCCTCTGTGA AAATGCATTT GTAAATGAAG 1380
GGAATACCTA CCAGGCAGGT GGTCAACAGA ACCTAGCACT 1420
|
