| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04561 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr13:47066520-47067970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:47067253-47067272 | AGACCACAAGAGGGCACCA | + | 6.8 | | ONECUT1 | MA0679.1 | chr13:47067418-47067432 | AGTATTGATTTATT | - | 6.06 | | ONECUT3 | MA0757.1 | chr13:47067418-47067432 | AGTATTGATTTATT | - | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AACAGATCAC ATAGTGCAGT GAAAAAGGGA GAAGAATCTT GGAGTCCTTG GAGACAACTA 60
CTAGTTTTTC ACTGTTCTTT GCTTCCATAT GATTTTCTGC TTTGCTCTTC AGTTTATAGT 120
AATTCAATCG ACATTTACTG CAACTTTGTG CTAAGCATTG GGTGGCTGGG AATATGTAGT 180
TACTTCCTCA AGACCAAAAC TCTGTGCTCA AAAGCACAAC CATTAGTGAC GGATTCGGAT 240
AAATACAAAG CAAAGTACAA TCAGTTGTCA GCCGTTATAG AGACTGGGAG GAGGTAGAGG 300
CACCAAGAGA GAAATAGACA AATGTTTTTA ACCAAGGGGA CATGAGGATG AGGAGGACAT 360
GAGAGAGAGG AAAATGAAGT TAAATTTGTG GGCTGGATCA TGAAGGTCCT TATATGACAC 420
ATGGATGTGA TCTAGCACTA TGGAATTATA AAAGGGTTTT AATTCTGATC TCATGTATGT 480
TAATTCTCTT TCTTTAGAGC AACTCCGCAG GACTCAAATA CATTCCTGGG TTACCAACAA 540
AGACATCACA ACCACCCTGA CTACATCTTT GGCAGGTAGG ATATTCTGAT TTAAAATTGT 600
TTAAAAGCAT GGTTAGTATC AGAAGCAATG AGTCTCAAGG AAGCAGTTTT CCTCCAGAGA 660
GAAGCAAGAT GCTATTTCCT GGATCCAAAT TTCCCAGGAC AAAACTTCTT GCATTTCTCT 720
TTTAAAAAAT GGAAGACCAC AAGAGGGCAC CAAACTTCAT CTTTCCGGCT GAGAAAACAG 780
CATCTGGGCA TTGCAAAGTA CAAAATGAAG AGGTGGCCAA AGGAACAAGT TGTTATTGTT 840
TGTCTTTGTT CCCTAATAAA ATTAGAAACA TATCTTTATA TTACTTTGCA TGAATGTGAG 900
TATTGATTTA TTCTTCAAAC TCCAAATCTG GGTTTAAAAA CAACAAAACA AAATGATACA 960
GTATTTTCTT TGCAATTGGA TTCCCACCCA ATATTCAAGG ACTGACGAAT AAGATAATGA 1020
ACCATCCTCT TCCTGATACT TGTTTTCAAG GCTGAGCAAC CTATAACTGC TGATAGGTGG 1080
CTTGTTCATT TATTTATTTA TTTATTTATT TGAGATTGAT TCTTACTCTG TCACCCAGGC 1140
TGGAGTGCAG TGGCACCATC TTGGCTCACT GCAACCTCTG CCTCCCGGGT TCAAGCAATT 1200
CTTGTGCCTC AGCCTCTCAA GTAGCTGGGA TTACAGGCAT GTGCCACCAC ACCCAACTAA 1260
TTTTTGTATT TTTAGTAGAG ATGGGGTTTC ACCATGTTAG CTAGGCTGGT CTCGAACTCC 1320
CTACCTCAGG TGATCCGCCC ACCTTGGCCT CCCAAAGCCC TGGGAATACA GGCGTGAGCC 1380
ATTGGACCCA GCCTGTTTAT TCCTTTAACA ATACTTATTC AGGTTTGGTG ATATGCTGGG 1440
CAAGTTGCTA 1450
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