| Tag | Content |
|---|
EnhancerAtlas ID | HS173-12726 | Organism | Homo sapiens | Tissue/cell | SH-SY5Y | Coordinate | chr7:4045830-4047280 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr7:4046549-4046560 | GGGCGGGAAAG | + | 6.32 | | SREBF2 | MA0596.1 | chr7:4047214-4047224 | ATCACCCCAT | - | 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 |
| GH07I004006 | chr7 | 4045698 | 4047150 |
| Enhancer Sequence | AGCTTTTTCA ACCAACAGCT AAAGCGGGGT TGTGATTCAT TCCTCGTGAT TCTCGGCCTT 60
ACCACTAAGA AAACGAAAGT GTAGTGATGC CCTCTGTAGA ACGGAGCCTG GCTGGGGAAG 120
TGTAAAATCC CTCAGTCTTC TAGATCTGAG AGTCCCTGAA GGGGAGGAAA AAAGGTATTA 180
AACGTTTATG GGATGGTTTC CTTTATCAAA AGATTCTTCT ACCTCCCAGC CTCCAAGACA 240
AGCATCCTGT GGCCCTCTTC TGTGAGGACC GGCTGGGGGC GGACCCTTTT AAAGGGATGT 300
TGCTTATTGA TTGTCAGGAA CAGACTTGCT ATTTAAATTT TAACAGTTCT CAGCAAGCTT 360
GCAATTCCAG AGCTTGAGAA TGAGCAAATC CTTCCCAAAA CAATTTTTTT TTGTATGAAT 420
CAGGGTGCCC AGAGATGGAT CAGTTCATTT GTATTAGTTT TCACTTTAAT CTCTCTTCCA 480
GCCAGACCTT TTATTTTCTA GTGAAAGAGG AAAAAGAATA AAGAAAGAAT TCCTATAGCT 540
GCAGCAGGAC TGGGCAGGCC CCGAGATGCA GAGGTAATTA ATAGGCCCTG TTGTCAAATC 600
AAACCAGGCA GCAGACTCTG AACCCTGAGG CTGGGGTTCT GGACTTTCAG GAGCTGTTTA 660
CACTCGGAGT GAACAAACAG CCAGGATCAG GCAGGGCCAG GCTGGCGGGA TGGGGCCGAG 720
GGCGGGAAAG CGGCGTCTCC AGGCTTGCTC TGCCTCTCCC GCAGTCTGAT TAATCGCCTC 780
AGTCACCTGG TTTCAACAGT TGTCCTCTTG ACTGTCTCTT TCTGAAACGA TGTTTGTTCA 840
CTGTGCCTGA CGGAGCAGGT GAATGGCTGA CTGCTAGACA CTGTGATGTC TGAAGGAAGA 900
AAGGGATGGA CGAAGAGCTT TACTGAGTCC AGTATCAGTC AAGCTTCCTG AGGGAAAAGA 960
TGGCGTTCCT GAATGAGAGC AATCAAGGAG GAAGTTTTAG AAGGGGAATG TTTGCAGAGG 1020
TGCGGGTGGA GGGGAACCAC TGTTACCGGG GGCTGGTAGC CTCAGAGCGG GTTTCACTCT 1080
AAGGTTCAAG AGCCCGAGGC AGTTGCAGAA CCCCAGAAGG AGAGATTATG TAGGGTGGCT 1140
GCTTGGAAAA GAGGGGGACC CAGGTAGCCC CAGGCAGCCT CCCAGTGAGG AAGAAAGAGC 1200
CTTACATTTG CTCCCCTCAT CTACAGGAAG CCTCGGGGCA GGAGTCCCGA GGACAGAGCT 1260
GGATAGGGAG GGCGGAGCTT GGATCTAGGG AGAGCAAGCT GTCCAGCACC CTGGGCCAAG 1320
CTTACAGCTA GATGCTTTCA ATGTATGTGA TTTCATACTC GGGGAGTCTT GGGGGTTATA 1380
TATTATCACC CCATCTTTTC ATTATTTCCT TTAATTTGTT TTTTGAGACA GAGTCTTGCT 1440
CTGTCGCCCA 1450
|
| |
|
|
|
