| Tag | Content |
|---|
EnhancerAtlas ID | HS184-28273 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr7:75795540-75796610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLIS3 | MA0737.1 | chr7:75796513-75796527 | CTTTGTAGGGGGTA | - | 6.51 | | NRF1 | MA0506.1 | chr7:75796011-75796022 | GCGCATGCGCA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 75796419 | 75796600 | | chr7 | 75795833 | 75796053 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I076162 | chr7 | 75791992 | 75796918 |
|
Enhancer Sequence | GTTTACTTCA GTCTCGCAGG ATAGAGTGCT GTGATGGGAT CATAGCTCAT TGCAGCCTTG 60
AACCTTGGGG TTCAAGTATC TGGGAAGCTG AGGAGGGACT ACAGAGATGG AGTCGCGCCA 120
TGTTGCCCAG GCCGCTCTTT AACTCCTGGC CTGAAGGGAT CCTTCCGCCT CGGCGGAGCC 180
CGGACATAGT TTTCTAGTTT TGACCCACAG AAACACTGTG CTGGGTCGGA GTTTGTCAAC 240
TACCCTTCTC CAGCCAGCAA CACACAGAAC ATGGCGGGGA AGTCACGGTC ACCAGGCTCC 300
AAACCGAGGA GAAAACAGCC CAGCTCCAGG CACTGTAGCG TCACTGTGAC ATCGCCGAAG 360
GCCGGCGCTA TTACGTCGCC GGAAGGCCCG CGCCTGTGAC GTCAGCGGAG GCGCGCCCCT 420
TCTGTAGAAC CAATCGGAAC TCGAGGCGCG GCGGCTGGGT ATTCCAGGAG AGCGCATGCG 480
CAGACGCGTG GCCACAGACT GCCGGTCAGT GTCAGTAGGC GGCGGGTTAG TGTCCGCAGG 540
CTCCGACTCG GCCGCCGACA CCAATAAGCT ACAAGGACGA GCTTTACCAC TGCCTGTACT 600
ACTGCTACCT GCGCGACTTC CCAGCCTGCG GCGTAGGGCG CAGCAAGGGC CTGACGCTGA 660
GCGAGTAGGC GCTGCGCACC AAGCGGCTGT GGCCCGGAGG GCACTGTCGG GCAGAAGCTC 720
CTCAGTGGCC ACCACAAGCC CGCTAGCTCC GGCTACAGCC CTTGCCGCAC ACTCGCGTCA 780
CCTGAGCCTG TGTAGGTGCG CCCCCCCAAC TCCTCCCCCA GCCAGGTCCC GGGGACACCG 840
GCAGCGTCCC CCACCGCCCG GCGCCGCTCA TTCTGGGCAG GATCGGCCCC GTCTGAGGCT 900
ACACCGCATT AGGGAGCTGC ACCCCTCGGC TTGACCTCTC ATGGCCTTTG CAACAACATC 960
AAAGCCTTTG GAACTTTGTA GGGGGTACGA GGGGCTAGGA AACCAAGAAA ACATCTCTTT 1020
AAAAATATAA GCGATCGGGC CGGGCACGGT GGCTCACGCC TTTAATCCCA 1070
|
