Tag | Content |
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EnhancerAtlas ID | HS093-18138 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr2:173378110-173379540 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr2:173378682-173378692 | TTTAATTAGA | - | 6.02 | SPIC | MA0687.1 | chr2:173378725-173378739 | AAAAAGGGGAAGGA | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 173378536 | 173379180 | chr2 | 173379222 | 173379297 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I172513 | chr2 | 173378529 | 173379728 |
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Enhancer Sequence | ACTGACTGAT CAAGGCCGCA GTCACAACTG TTTACAGCAC TCTGCTTGTA GTCTGTAAGC 60 AGCCTGGACA CTCAGCTGGA CTGGCAAAGC AGCATATCTG TGTGTCAGTG TACTTTATTC 120 ATCCGTTGTT GGGTCAGGGT CTGTGGGACA GACTCCGCAG CTGGTGCCCT GTGTGGGGAT 180 CGCTGTGAAG GGAGCGCGAC AGACCCCCAG AAATGAAGGT GGAGAGGACT GGCGGTCAAG 240 TCAGTAAAAC AGTGAGTCAT TGGTGCCTGC TTGGGATTAC CAAGTTTGGG GGGGTGGGGG 300 ATTGTTCAGG CTGAGATTTC ATCATGGGAC AATAGTTATC AGTTCAACAA AGACAGTACA 360 TAAAAGTGTT GAAACAGTTA CTTAAGGCTA GGGGAGCATC AGTTTTGCAG GCTCAATTAA 420 GAGACCCAAT GCAAACTGTT GTCTCACTTA ATCCATGGTT CCCAGAAGAA GGACCGCTAG 480 ATGTAGAGGT CTGGGAACAA GTGGGGAGAA ATATTAAACA ACGTTATGCA CAAGGGCAAT 540 GTGTCCCAGT AACAGCTTTT AATGCTATGG GCTTTAATTA GAGCAGCCCT AGTTCCGTTA 600 TACACAGAAG AGCCTAAAAA GGGGAAGGAG GAGGAACCGT CACCTATCTT ATCGCCTCCT 660 CTTCCCTCAG CCCTGATATT ACTGGGCCAA AATAACAAAG AGGAAACAGA AGTTGTGCCT 720 GAGCCACCTC CTCCAATAGA TAAGAAAAAA AAAACAAAAC AAGAGATACA CTACAGCTAT 780 GAAACCCTGT CTTAAGCAGG CAGCATTAAA AGGGGAGCTC TTAGCCTGCC CAATAATGCA 840 AAATCAGCAA GGCAATCAGG TACCTAAAGA GTTGTTAAAA AAAAGCATTA GAGGCCAAAG 900 CCAGGCGGCC AAGCGAGCAG TAAGCAGAAG GAGAGACTTG GCAGAGAGGA AGTTCGGGAA 960 ACCAAAGCCA GCAAGTGCTC CCAGGAACTC TGTCCACACG GAGGCAGCGG CAACAAACAG 1020 CCAGGCCCAG TGCTTGGAAG TTAGCCTGTT AGAGAGAGGC AGGAGGCGCA TGTGGGAAAG 1080 TCGGCCCAGT GGGCAACAGC CACTGGGCAG CGGGGGTAGG AAGTGGCACA GGCGAAAAGC 1140 GGCACAGAAA AAAGCAGCGC TTTTGCAAGC GCAACACAGC TGCCACTCCA GGACCAGTCT 1200 GCTTAGCTCT CCAGCTCTGC AGGTGGCCCA CGGCAAAATT TCATGTGCTC CTTGTAGACA 1260 AGAGACATCC CAAATTATAA TTCTATGCTA AGATTTAAGT AAAATTTAAT AATTTGAAAA 1320 ACCTCTTTCT GATAATGGGC ACTGTTATCT CTCTCTTACC CCTAACTCTC TCCAAATCCA 1380 ATTTAAGTAA AACTGTAACC TCTAAAGGGA GAGAAATTAC AAACGGCCCA 1430
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