Tag | Content |
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EnhancerAtlas ID | HS067-00169 | Organism | Homo sapiens | Tissue/cell | GM18522 | Coordinate | chr1:32963790-32965130 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:32964515-32964525 | TCTAATTAAA | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGCCATGAT TGCACCACCA CACTCTAGCC TGGACAACAA AGTGAGACCC TGTCTCAAAA 60 ACTAAAAACA AGGCCGGGCA TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG 120 AGGCAGGTGG ATCACCTGAG ATCAGGAGTT CCAGACCAGC CTGGCTAACC TGGTGAAACC 180 TCGTCTCTAT TAAAAATACA AAAAAATTAG CTGAGCGTGG TGGCGGGAGC CTGTAATCCC 240 AGGTACTTGG GAGGCTGAGG CAGGAGAATC ACTTGAACCC AGGAGGCAGA GGTTGCAGTG 300 AGCCGGGATT GTGCCATTGT ACTCCAGCCT GGACAACAGA GCGAGACTCA GTCTCACAAA 360 AAAGAAATAA AAATAAAAAA GTTTTGAGAA TAGTTTTTAT TTTTTATTTT ATTTTTTTGA 420 GACAGGATCT CGCTCTGTCA CCCAGGCTGG AGTGCAGTGG CATGATCTTG GCTCACTGCA 480 ACCTCTGCCT CCTGGGTTCA AGTGATTCTC CTGCCTCAGC CTCCTGCATA GCTGGGATTA 540 CAGGCGCCTG CCACCATGCC CGGCTGATTT TTGTATTTTT AGTAGAGACA GGGTTTTGCC 600 AAGTTGGCCA GGATGGTTTC GAACTCCTGG CCGCAAGCGA TCCACCTGCT TTGGCCATAC 660 AAACTGCTGG GATTACAGGC ATAAGCCACC ACGCCCGACC GAGAATAGTT TTAAGAGGAT 720 TTGTTTCTAA TTAAAGTGAG TGACTTTACG ATCATTCTGG GAGAGGAAAT CAGCAGATCA 780 CCTGGAATTG GAAAGCAGGG CTGAGGCTGC TCCTGGTCAG TCATGTGCCT TGCCCATGTT 840 TCCTGTACAC TTCTCTTTGT GCCTGTGTGG GGTCCCCGGC TACTCTCAGA AGACCACCTT 900 TCTCCTGCCC ATTCCTCAGC TCAAAAGTGC TGCCCAGCCC TGACCTAACC ACTGTCCTGT 960 CCTTCAGTCC AAATCTTCCA AAGGAAAACA CCTCAGTTTC TGCCCAGCAA AAGATCGGTT 1020 CCCTCAGATC ACATGGCACC CCTTGGGTCA GGAAGCATGA GGCTCTGACT AAGGATGAGT 1080 GGTGGTCATG GGGACAGGTC CCCTGAGAAG GGGCCCTGGA GAGGGGCAGG AAAGTTGACC 1140 TACATGTCTC CTAAATAAAT AAAATCATGG CTGGCAGGAA ATTTGAGAGG AATGCACATG 1200 ATATACTTCC AGGAGCTCCC AGAATTAATG GGGGAAAAAA CTGCAGGTGG CTGTAGAGTT 1260 TTCCATTAGA AGGAGAGTAA AGTGTATTTA GTTATTTGAA AACAGGTGTT CAAACTGAAA 1320 CTTGTACACA AAGGTTCATA 1340
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