| Tag | Content |
|---|
EnhancerAtlas ID | HS150-06781 | Organism | Homo sapiens | Tissue/cell | NT2-D1 | Coordinate | chr20:49486870-49487980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr20:49486963-49486977 | CCAGCCGGGGCCTG | + | 6.11 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH20I050870 | chr20 | 49486635 | 49488526 |
| Enhancer Sequence | CAGCACAGGG CAAACGGAGG CCCTGAGGTG GTGGGCTTGG CTTTAGAGCA GAGCTTGTTC 60
TGACTGGGGG GCTTCAGAGG AGAGGCTGTG AACCCAGCCG GGGCCTGAGG CTTCACCCTG 120
TCACGTGCTG TGACAGCCAT TTGGGGTCTT TGTGAGAAAC GGAGCTGCTG GGTGTTGCGG 180
ATTGCCGGGG CCAACTCTGA GGCTTCGGCC AGACGCAGCA GGTTACAGGA ACCGTGGGGA 240
TCTCAGGCTG GGGCTCCTCA GCTCAGCCAC CCTCAGCCAT GAGGGACTGT GGGCCCGGAG 300
TTGCCCAATG GTCTGATTTT CCAAGAGAAA CCGGCAGTCT GCTTTTCACG GGAAATCTGA 360
TTTTTACATG TTTGCAGTTA ATTCCATTTT TACAAAATCA CAAAGCCGAC CCAGCACACA 420
TGCATTTGGC CTGTGCCCTG CAGGTCTGGG AACTCAGGTG CGCAGGGTGG ACGCAGGGAG 480
CTGCGGGGGT GTGGGGAGAC TCTGAAAGCA GCCAGGCCCT GCGCCCCAGC ACTCCCTGTG 540
GCAGAGGCGG GCCTTGGGCT GGGGGTGGGC TGCGGAGGAG CTCACAGCCG TGTCAGGTTT 600
CTGTGTCTTG ACCTATCCTA TCCCAGAGCA GAGAACATTC CTGCCTGCGG CCCGGGAGGA 660
GGGGGTGGGG AGCTGGATTC CAAAGGGTTG GACGCACCTC CTGGACCCCA GCGGGGACTC 720
ATTCCCAGCC GGAGGGCGAG AGGTGGGACG TGGAGAGCTC TGAAGTCTTC TCTGAGATTT 780
TCAAAGGTGA AAACCCCAGG GTTTGAGTTT GCTGCTCCAT CCTCAAGGAG CCCTAGAGGG 840
CGATGGGCAA GGGCTGGTCT TGGAGCTGGA CAGGCCGAGG GGACCCCAGC TCCAGTGCTC 900
CCTCCCTCCC GGGACCCCTG AGACATAGCG ACTCCTCCCT TGCAGGCTGC CATGATAGTC 960
CAAGAGAGAA CGGGTGTGAA AGTGGTTTCC ATGGCATGCG GGTGTGCCGG TGAGGGGGTC 1020
TGCCTCTGGG AAATGGTCCT GTCCACCCGC CAGGGCGTCT GCAGCCGGAC AGCCCTGCGG 1080
GCATCTGGTT GTTTTCAGCC TCACACACCA 1110
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