Tag | Content |
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EnhancerAtlas ID | HS098-48179 | Organism | Homo sapiens | Tissue/cell | HSMM | Coordinate | chr6:33570780-33571940 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PBX1 | MA0070.1 | chr6:33571047-33571059 | CAATCAATCAAA | + | 6.18 | PBX1 | MA0070.1 | chr6:33571043-33571055 | CCATCAATCAAT | + | 6.62 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCATGCAAAC TCAGAGCAAG AACTCACTTA TCACTGCTAG GAGGGCACCA AGCCATTCAT 60 AAGGGATTCA CCCCCATGAC CCAAGCACCT CCCACCAGTC CCCACTTCCA ACATTTGGGA 120 TTACATTTCA ACATGAGATT TGGAGGGGAC AGATATCCAA ACCATATCAC ATTGCCCCAT 180 GACCCCCCAA TCTCATATCC TTCTCACATT GCAAAACACA ATCATTCCTT CCCAGTAGTC 240 CCCAAAAGTC TTAACTTGTT CCACCATCAA TCAATCAAAA GTCCCAAGTC CCAAGTCCCA 300 AGTCCAAGAT CTCACCCGGA GATGAGTTTC TTCCACCTAT GAGCCTGTGA AATCAAAGAC 360 AAGTTATTTA TTTCCCAGAT ACAATGGTAG TACAGGCATT GGGTAAACAT TCTTATTCCC 420 AAAGAGAGAA ATTTACCAAA AGAAAGGGTC AAGACATCTC ACACAAGTCC TAAATCCAGC 480 AGGGCAGTCA TTAAATTTTA TTTTATTTTA TTTTATTATT TTTTTTTTTT TTGAGACAGA 540 GTCTCGCTCT GTCCCCCAGG CTGGAGTGCA ATGGTGCGAT CTTGGCTCAC TGCAAACTCC 600 GCCTCCCAGG TTCCAGCCAT TCTCCTGCCT CAGGCTCCCA GGTAGCTGGG ACTACAGGTG 660 CCTGCCACCA CGGCCACTAA TTTTTGTATT TTTAATAGAG ACGGAGTTTC ACCTTGTTGG 720 TCAGGCTGGT CTGGAACTCC TGACCTCAGG TGATCCACCA CCCTCAGCCT CCCAAAGTGC 780 TGGGATTATA GGCATGAGCT ACGGAACCCG GCCCAGTCAT TAAATCTTAA AGCTCCGAAA 840 TAATCTCCTT TGACTCCATG TCCTACATCC TGGGTAGCTC TGCCCTTGTG GCTTTGGAGG 900 GTGCAGCCCC TGTGGGTGCT CTTCGTTGAA GCTGAGTGCC TGCAGCTTTT CCAGGCTCAG 960 TATGCAAGCT GCCTGTGGCT CTACCATTCT GAGGTCTGGA GCATGGCAGC CTCCTTCCCA 1020 CAGCTCCACT AGGCAGTGCC CTGATAGGGA CTCTGTGGGG ATTCCATTTC CACATCTTTC 1080 CTCCCCTGTG GCAGGCTGTA CCTCTGTGGC AGGCTTCTGC CTGGGCACCC AGCCGTTCTC 1140 ATACATTCTC TGACATCTAG 1160
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