Tag | Content |
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EnhancerAtlas ID | HS150-00986 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr1:165322500-165324720 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:165322846-165322861 | AATTAATTATTAAAT | + | 6.39 | Lhx3 | MA0135.1 | chr1:165322845-165322858 | TAATTAATTATTA | + | 6.18 | MEF2A | MA0052.3 | chr1:165323958-165323970 | GCTAAAAATAAA | + | 6.04 |
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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 | TGTAGCCACA ACAGACGTTG GCGGGTGAGC AGCCCGGGCA GGTAGACCAT GCCAAACCTG 60 GCCGGGACCC GCTCCTGATC CCTTCACATC CACGGATTCC CCCAGCGCCC CCCACCCCAG 120 GGAACTCCTG CTAATCAACC AAGCTGAAAC CTGGAAAAAA TCAAGCCAAG TGGCGTTTCT 180 AATAAACGGA GACTATGTGA GAAGGTTTAA TTCCAAGCGG GGGAGGGTAT AGAAATCAAT 240 AATTGGCCTT TAATTAACAA ACATACCCAG GTATGCTCGC AAACGTCTGC ACATCCTGTA 300 AGATTAAATT ACATACAAAT TTGTGCTCTC AGGTTTATTA CGTCGTAATT AATTATTAAA 360 TCACTATGCC TGTCTCTACT GACTGTTTTA AAAACTGAGA ATGCATAAGA ACAATTTGGA 420 TTTTTCTTTG TTAAAACGCA GAGTTCTGTT CTATTTTTTG AGGGGGAACA AAATTTTCTC 480 TTTTCTTCCT AAAAAGTCCT GGGGGTACAG AAAAATACCG TCTCACTCCG AAGCAAACCT 540 AATATTATTC AAACCGATGA ACCCCAAACT GCTGCGTCTT GACTGGCATG CATATTGCAC 600 ATGGGTTTTT GATAACTAAG AAGCGTCAAA ACAGAGGGAG GGAAAAAAAT AGCGGAAGAA 660 GCAAGCCGCT GAGTGTCCCG GCCGGGATTC CCGATGCCAG GCGCGTTCGG CAGCAGTGCT 720 TGAGGGCGAA ACGGGCCTCA AAGTGACTCA GCGGAGGCAG GAAATCCACT CTTTGCTACC 780 CCTTGGACTT TGTGTTTTGT TCCTTTAGTT TGTGGGGGGC GGAGAGGTGG TTCAGGTGGC 840 GACGCTTGGC CACCTATATT GGCACTTTTC ACAGCTATTT AAAGAAGGCC TTGTCCCCCA 900 GCAACAACAC TCTTGCCCTT GTCCCCCCAG TACCAACACT CTTGCGCTCC CCATTTCCCG 960 GCTGCACTCT TCTCATTCTC CCCTTCCGAG AGGCCCGGCC ACCGGCTCGG GAGCTGGGCC 1020 GGTCGCTTTG GGAGCGGATG AGGAAGGTTA GGAGAAGCAG CGAGATAGAT CCCAATTTTA 1080 CAATTCTATT TTCTTTCGGT AGGGTCTCGG CGTCCTGGGC CACGTTGAGA GCGAACGTGG 1140 GCCGAGCGGA GGACACAGAG TAAAAAGCGA CGCCCGCTGT ATACATAAAT CCGCACCCGC 1200 TGCCCGCCCG GGTACTGCCT GCTCTGGCTT CCGCTCTCTT CCGAGGCTGG GCAAGTCCAA 1260 AAGTTCCCGA AAGGGGGGTT CAAAGAGGGG CGCTCAGTGC ACGTGATTTC GTTTCATCTA 1320 GGGTGTTGGG GGTGGGGAGA TTCCTCACTG GATTTGGTTT CTCCAGCAGA ACTGTCTCAT 1380 CCTCCACATT CATGCCGCTC TAGCGGTTCC GAGTGAAAGA GGCAAGAGGT TTAAAGGACA 1440 GAAGGAAAAC TCCCTCCTGC TAAAAATAAA TAAATAAAAT AAAATAAAAT AAAATACGGG 1500 CTTCCCAAAC TTGAAAAGCT CCAAGGGCAG AGTGGGTGGG GGAGCCGTAA CCAGAATCTC 1560 TGGCTTCAGC TCTGCAAGAC CCGTGTGTGG ACACTCTTCC GGGGTCCTTG ACTCGCTGCT 1620 CCTCCTCTGT CGCTGCAAAG GAGTTGTGAG GGGGGACCCA CAGGACCCGA CATCCAGCTC 1680 CAGTTAATTA ACGCGGAGCC TAGGGCCCAG CCGCGCGGTC TAATCCCCGC GCTGCGTTGC 1740 CTACTGGCCC AGAAAAGTCT CTCTCGGCCT TGCCCATGGC TGAAATTGGG GCTGGAGTTG 1800 GTGGGGGAGA GAAGCCTCCT CGAACTTGGG CGCTCCAGGC CTCGGGTCTC GGATGCTATT 1860 GCCTCTAGGC CGCGAGAAGA GGGCGGCATT TATGAGACGT CGATCAGCTC CGAGATTAAA 1920 AATCCAGCCC TGGGTATTTT TAATCACTTG CCACTCAGAC GCCTACGAAC AAGCTCGCCC 1980 GCCCCTCGCG GCTTTGGGGA ATTCGGTGCC CAGTGCGTGA GGCCTGGGGC GGCTTGTTGG 2040 ATTTATTTGG GTAGGGACGA CCCACAAGCA CTGACGGACA GATAGTGATG GGGCTCAATT 2100 TAGTGTATGA AGAGGGGCGC TAGCTTCCCT ATCGCGGACC AGGTCCCAGA GAGCGGGGCT 2160 CCAGAGCTCA GCGCCAAGCG GAAAGAGAGT GCGCCCAGGA CGCACGGCCT GAACACTCAC 2220
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