| Tag | Content |
|---|
EnhancerAtlas ID | HS051-09562 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr15:78469500-78470950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr15:78470632-78470644 | GTTTGTTTGTTT | + | 6.32 | | HSF1 | MA0486.2 | chr15:78470346-78470359 | GAATCTTCTGGAA | - | 6.06 | | Myog | MA0500.1 | chr15:78470601-78470612 | CTGCAGCTGTC | - | 6.62 | | SCRT1 | MA0743.1 | chr15:78469925-78469940 | AGTCACCTGTTGCTC | - | 6.54 | | SCRT2 | MA0744.1 | chr15:78469927-78469940 | TCACCTGTTGCTC | - | 6.36 | | Tcf12 | MA0521.1 | chr15:78470601-78470612 | CTGCAGCTGTC | - | 6.14 |
|
| | 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 |
| GH15I078177 | chr15 | 78469821 | 78469970 |
|
Enhancer Sequence | GAAAATGGCC AAGAATAGCC AAGGTCATCT TGAAGAAGAA GAAGACCAAG GCTGTAGGAC 60
TTAGCCGGAT ATCTATCCCT GTCATAAAGC TATAGAAATT AAGACACTGG GTATTGGTGC 120
ACGGATAGGC GAATAGACCA AGGGAACAGA ATAGAGTCCA CACATAGACC TCTCATAGAC 180
AGTCACTTCA TAAAGGACAA AGGTATCACT GCAAGGCCAT GGGGAAAGGA TGCTGTGTCC 240
GTTGGATATG TATTTGGAGA AAAGCTATTT GGACCCTTAC CTCTCACTAT ACTAGTTCTA 300
AAAGGAGGGC CGGCTCTGGT TGAATTTGGT TTTCTGGCTA CTATCCTCCC CCATGCAGGG 360
ATGTGGGTCC CCTCATCGGC CATTACAAAG AGGCACACTA GGCGGCGCCC ATGGCACATC 420
CAAGCAGTCA CCTGTTGCTC CCGGGGTCTC ACTGGAGGGT ACCTCCAGGG CTCATCAGCC 480
TGCACATCCC AGGGCCCAAA CGCCACCGCG ACCTTTTGTC CCTCCCTGGG GTGGCCGAGC 540
CTCCATGGCC ATCAGTTGGG TCCTGGGCAT GGTCGCACAC TGCCTGCATG ATGTCCACAA 600
AGTAGTTTAC CCACTCAACT TAGCTTCAGT TTCCCCCATG AAGCCCTGGT GCAGGATTCC 660
CACGTGGATG CTGCGGGCAT GACACCAACT TGGGTGAAGC AGGCAGAACA TTCTTCCACA 720
GAGGCATCCC CAACTATTTC TGTCTCTGTG GGAAGTTTGT CTTATTTTAA ATTTTATATC 780
CAATTTGCAT TCTATTCCCC ATCATATCCA TGTTTGCATA TAAAAATACA TAATACTTAC 840
GCTCCTGAAT CTTCTGGAAA GACTTGCCTT GTTTCTCTAG GGGTCTGATT TCCAGCTCTG 900
CCATTTACTA GCTGGGTGAC CTTAGGCAAG TTACTTAACC TCTCTGGATG TCCTCATTAG 960
CAAGTTAAGG TTAATAAGTA CCTGCCCCAT AGGAGAGTGG AGTAAATAAA ACGATGTCAC 1020
TAAAGGTGCC ATCTTAATAA AGGCTCAAGA CCAGCAGCTG GTGTAAACAG TGCTGGCAGT 1080
GGAATTCCTG CTCCCACCCC ACTGCAGCTG TCCAGGGCGC TTGCCTTTTT TTGTTTGTTT 1140
GTTTTGGTTT TGTTTTTGGA GACAGAGTCT AGCTCTGTCT CCCAGGCTGG TGTGCAAAGA 1200
GGCAATCTCA GCTCACTGCA ACCTCTGCCT CCCGGGTTCA AGTAATTCTC GTGCCTCAGC 1260
CTCCCGAATA GCTGGGATTA CAGGTGCATG CCACCACGCC CAGCTAATTT TTCGTGTGTT 1320
TTTAGTAGAG ATGGGGTTTC GCTGTGCTGC CCAGGGTGGT CTTGAACTCC TGAGCTCAGA 1380
CAATCTGCCC GCCTTGGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC ACCGTGCCTG 1440
GCCTGGGGTG 1450
|
