Tag | Content |
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EnhancerAtlas ID | HS108-11022 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr13:20410350-20411330 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr13:20410351-20410362 | AAGCAATAAAA | + | 6.32 | ONECUT1 | MA0679.1 | chr13:20410356-20410370 | ATAAAATCAATAAT | + | 6.53 | ONECUT2 | MA0756.1 | chr13:20410356-20410370 | ATAAAATCAATAAT | + | 6.59 | ONECUT3 | MA0757.1 | chr13:20410356-20410370 | ATAAAATCAATAAT | + | 7.01 | Stat4 | MA0518.1 | chr13:20410996-20411010 | CTTCTAGGAAATGG | + | 7.04 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | AAAGCAATAA AATCAATAAT AACTTCCCTA AAGACATTTA ATAACAACAG ATAATGAACT 60 TTTTTTTTTT TTTTGAGACA AGTTTTTGCT ATGTTGCCCT GGGCTCGAAT TCCTGGTCTC 120 AAGCAAGCCC TCTACTCATG CCTCCTGAAT AGCCCAGATT ACAGGCTTGC AGCACCACAC 180 CTGACTTTGG TTTAGAAGAT TTTGACATGA CCCGCTTAAA GGAAATGGGT CAACAATCTT 240 TTTTTTTCTT TTGATAGTGT CTCTTGCTTT ATCACCCTGG CTGGAAAGCA GTGGTACAAT 300 CATAGCTCAC TCCACCTCAA ACTCCTGGAC TCCAGTGATT GTCCTGTCTC AGCCTCCTAA 360 GCAGTTGGGA TTATATGTAT GAGTCACTCA TCAACAAGGA TCAACAATTT TTAGATGGTA 420 TTGTAAGTAA AGTTCACTGC CCTAGAACAT TTGTGGAGGG AGCTAAGGGA ATCAATATTA 480 TCTGTATTCA GGATCGTGTC TGTATAACCA GAAGCAGGGT AGTTCTCACT GTGGTAACTG 540 AGATAAAATC ATGTTCTTGA TATGCATGAC TCAGGGGTAA CCAACACCAA ATTTAGTTAC 600 CAAAGACTTT TATAAAGTGA GGACTGCCTG CATGCATGTT TCTTCTCTTC TAGGAAATGG 660 GAAGATTGCA ATATCACTGA ATGTTAAGCA AACAGCATAC ATTCACTCCA CTTGTTCCAT 720 GTGTTCTTGT ACCGGGATCT GCTGCTTTCT AATTTTAACT TTTAGATTCA GGGAATACAT 780 GTGCAGGTTT GTTAGATGGG TATGTTGTTT TTTGTTTTTT TTTTTTTCTT TCTTTTTTTG 840 AGACAGAGTC TTGCTCTATC ACCCAGGCTG GAGTACAGTG GCGCAATCTC AGCTCACTGC 900 AGCCTCCGCC TCCCTGGTTC AAGCGATTCT CCTGCCTCAG CCTCCCAAGT AGCTTGCGCC 960 ACCACACCCA GCTAATTTTT 980
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