Tag | Content |
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EnhancerAtlas ID | HS051-14390 | Organism | Homo sapiens | Tissue/cell | Fetal_thymus | Coordinate | chr19:45458720-45460350 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX2 | MA0700.1 | chr19:45459321-45459331 | GTTAATTAGT | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TCAGGTACGG AGGCCGAGAG GGGACTGAGG GGGTTCTTCC CCAGCCGGGG GGCCTCCCAC 60 GGGGCGTGTC CTACCTCTTG TCACGGAATC CCGTGCACTG GGGGCTCCTT GGCCAGAGGG 120 ACCTTGAATA CCCGGCCCAG GCAGGGCCGG ACCGCCCGGG AGGCCGGACG GTGCCGGGAA 180 CAGGGCCCTG TTGCGGGTCG GTTCCCCTGC ACGCTCGAGC CGGGCGGCCA CCAGGCTCAT 240 TGCTCGATCC GGGGAGACAG TGGCTCGGAG GGGCGCAGGC TTGTACCTTG GCGCGCTGGG 300 TTCTCAACTC CGCGATTCCA TGCTCTGAGG CCGTTCCTAG AGTGGTCTGG CGTTCAGGTC 360 TCGTTGTAGT GTTTGAGGTG TGCGCAGTGA TTAATTGGGA GTTTTCTAGC TGTGGGGAAG 420 TCAGTATTAG CAGGGCACGG CCGACAGACC CATTTTACAG ACGGGAATTC AAGGAACAGT 480 GAGACTAAGG CGCTTCTAGA AGGTCATCCT GGTTAGGTTT GTAACTTTAT GTAGAAGTTA 540 CAAGACACTG CTGACACAGG GACTGGTATG GTTGTGGTTT TAATGTAAAA TAGTTCTATG 600 GGTTAATTAG TCCTGGTGCG GATGACTTCT GCCCCACTGC TGTCTTAACA CACTGCAGAG 660 CATACCATTT CAGGCAGCTA CCGTTCAGGC ATTTGGGGAA TAGATGGAGA GACATGAAGG 720 TGCTGTCGAC CCACCCACTG GGATGTCACT GACATGTGGG AGGCAGCTCA GGGGAAAGGA 780 GTGCGGGTTG AGAGGGGAGA ATGAAGCTGA CTCTCTGTGT GACCTTGGGC AAGTTCCTTT 840 CCCTCTTTAG GCCTTTATCT CTCCCGTGTT AAATGCAGAG GTTGGACAGG AGGGCCAGCC 900 ATATCCCTGC TGTCAGGGGA CGAAGAGAGG AGACTGACAT GTAAACAGTT GTAATCCTGA 960 ATGATTAGGT TGGTGACAAA AGTCTGTGTC AGGGACTGGG GGAGCCCAGA GAAAGAGCAA 1020 GTGGTATCAC TTGGGTAGGA CACATGGATG AAATTTGTGT GATAGAGCCC ACTGTATCTG 1080 CTCTGAATCT TTTCAGCATT CTCAGCCAGG GCCTGGCTTC AGGGACAGCT TAGGAAATGT 1140 TTGTTGAGTT AGTGCTGGAA TGAAGGCTCA GTTCCTGTCT TCAAGGGTTT CCCAGTCTTG 1200 CTGAAAGGAG GTCGTTTCCC CTCTGGGTTT CTGTTGATTA TTGGGTTGAT GGTGGCTTGA 1260 GAGACCAGGG CCCAGGTTGT TCTCATTGCC CTGAGCTTCC AGATGGCACT CTGATCTTCT 1320 CTTGTACCAA CTCTGCTTAA AAACAATCAA GAGTTACCCC TTTGCCTTTA GGACAAAGTA 1380 CAAATTCTTT AATAAATCAC AGTCTTGCAC GATCCGACAC TTTTCTTCAG ACTAGACTAG 1440 GATTTCTCGA GCTCGGCACT ATCAACATTT TGAATTGGAT AATGCTTTGT TTGGGGGGCT 1500 GCCCTGTGCA TTTTAGGATG TTTAGCAGCA TCCGTGGCCT CTACGCACTA GATGTCAGTA 1560 GGATCCACGC CCCTCCCCAG TTGTGACAAC CATATATGTC TCCAGACATT GCCAAATGTT 1620 CCAAGAGCAG 1630
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