Tag | Content |
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EnhancerAtlas ID | HS029-00455 |
Organism | Homo sapiens |
Tissue/cell | CUTLL1 |
Coordinate | chr1:39024570-39026060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF5 | MA0599.1 | chr1:39025500-39025510 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr1:39025525-39025535 | GGGGCGGGGC | - | 6.02 | SP2 | MA0516.2 | chr1:39024615-39024632 | ATCAACCCCGCCCCCTC | + | 6.35 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I038557 | chr1 | 39023613 | 39026505 |
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Enhancer Sequence | TCAGAGGCCC CCTCCCTTCC CCCAGGCAGG TTACCCAGCC CATAGATCAA CCCCGCCCCC 60 TCCCAGCCGC CTGGACAGGC CCCAGTGAGT TCAGGCCGGT AAAAAGGATG GGCTGGGAGA 120 GGACCAGGTC TCACGTTGCG CCCCGACTGT GGAGATCCAC TTCAGATCTG AGTGCAGCCA 180 TGAGGTTTTG GAGCAAGTGC CAAGTCCTGG GCTGGCGGCC CTCATGCCTT GAATCTCCGC 240 CACCCCCATA AGGACGTGGA GAGGTAGGCA GTCCCAGGCT GGTGATCCTA ACTGGTGTTT 300 TGCTGCTATT CACCGCATCT CAGGCCCCCG TTTTCAATGC TTAGCGCCGT GGCTCTTAAC 360 CCTCACGACA ACGACAACAT ACTCTAGAAG GCAGGCACTA CTAGGGCCTC TGCTTTACAG 420 GGAGGGGAAC TGAGACTGAG ACAGGAGTTA GCCAGGAAGC TGCGGGGCTG AGAGTTTTGG 480 ACACCGGCAG TGTGATCCCA GAGTCCAGGC ACTTAACCAT CAGGGCTCCT TCTGCTACGT 540 GCATTTTGCA GAGGAGGAAA CTGAGTCTCA GAGTGGTGCA GGGGAAGTCA CTGGCCAAGG 600 TCACGGAGCG CTTTTTGGCA GATCAGGAAG GTCAAGTCCG GTACGATTCT TCCGCTTGCA 660 GCTTCGTGTT GCTCGGTGCG CAGGGCAACG TCAGAGCACC TCTGACTCCA GGGAGGTGGA 720 AGCGGCTTCC GGGGTGAATG CGGTTGGATC GTGCGAGGCC GCCACCACTG CCAAGAAAAG 780 AAACACACCA CCGCACACCT TGCCATCCCT GGGTCACCAC TTCCTTCTTC GTGTATGAAG 840 AGCAGCAGAC GGAACTCAGC AATGTTTTTC TAACACAAGA AGGATGACTT TCCGAAATCG 900 TTTGAAGTGG GAAGACTGGG GCGAGCGGGC GGGGCGGGGC GGGGGGCGAG CGGGAGGGGC 960 GGGGCGGGGG CACGGGCTTC TTGTCTGAAC AGTGCAGTGG CTGCATGTTT GGGGTGAGCT 1020 TGATCTTCCT GTGTAAACTT GTTTCTAGTC TGCTATTTAA AACCTGGCAT ATGGATGGGA 1080 TCTCAGCTTC CAGTACTGGC AGTTCTTAAC ATTCACAGCG ACTAAATAAA AAGGGAATTT 1140 TAAAAACCAA ATGCAGTTTT ACCCCATAAT GAGGCAAAGA GAGAAGTACT AAGAAGTTAA 1200 CAACTCCCGA ACTCAGGCTC AGCCAACCCT GTAAATGTGG GGGCCTCTGC AATGCAGCGT 1260 GGGGTTCAGA GGAAAGGAAA CGACATTTTC TGAGTACCTA AGGTAGGCCT TAGCTTTTTG 1320 TGCTGGGGGC TTAGCCCCAG GGTTAGGATT AGGGTTAAGG GGATGGCCTT CGTAGTCAGC 1380 CACCAGGTTT TGAAGCCCAG CTCTGTCACT CACTACCTGA GTGACCTTGG AAAAGTTACT 1440 TTACCTCTCT GAGCTTCCTC AGCCCTAAAA CAGGCCTAAA AGCAGGACCT 1490
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