Tag | Content |
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EnhancerAtlas ID | HS087-00872 | Organism | Homo sapiens | Tissue/cell | HEK293T | Coordinate | chr1:45450720-45452160 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Zfx | MA0146.2 | chr1:45450721-45450735 | CCCGCCTCGGCCTC | + | 6.01 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ACCCGCCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCG CCCGGCCAAT 60 AATGTCCATC TTATGAGAAG CACTATATTT GTATTTGCTT TACTAGACAG AGACTAGATT 120 ATGGAAAACC TTCGTACTAA TTGAGCCATG CTGCTTCATA ATTCTGGTCT CTGCACTGCT 180 ACTGTTGCTT CCTAGTCTGC CTTTCTCTTG TGTCTAGTAA TCACCTATTA AACTTTGAAG 240 ACAGCTCAAG AATCCTCTTG CCTACAAAGC CATTCCTAAC CGTTCCCACC CCTCCAGAAG 300 TGACTCCTTT TCCCGAAGTG CTTCCATTCT GCCATGTGCA GATTCTCTTA GCCTTTACGG 360 GTTTCATTGC ACGTATGTGT TTAAATGTCT ACTTAAGTGT AACATTAATG TCTCTTAAAT 420 GTCTACATAA GAGTGTAAGA GTGACTTTCT TGGACTGTGT GTGCATCATC ACTGTATTCC 480 CAGTCAGATG CCAGAAATCA AAGTGGAATG AGGACCTGTG AACTTCACAA CTGTATAAGA 540 GTCAAACTCA AACATGTGCA TAAGGGCATT AGAACCCAGG TCACTAGGAA CTGAGGTTCC 600 AGCTCTCAAG GAGGCCCTGG GTGAAGAAAG GCAACCTAGG AAGCATGAAT AGTAATCATG 660 AACATAACTA ATCATGCTAC CAGGCAGACT GTCAAATGCT CATGTCACTG CCACGACTAT 720 GGCTGACGGG AATCATGGCA ACGAGTCTCG CTGCCTCCCA AGCTTTGGAG AGGGTGTTCA 780 CCGCATCTCA GACTTGCCTG CATCATAGCA CTCATGCCTT TTCCAGTTGT AAATAGATAA 840 GAAAACTGTA TCAGAATTGG TCTGTCATTC CACGTGTGCT GCCTGAAGGC AGAGACCTCA 900 CTGCTCCTCC CTATATTTCA CTGCCCTGCA TCCAAACAAC TAAAGGCAGG CTGAACAAAT 960 GAATGAAGGG CTGAGGCTGA AAGAGTGCAG GCACAGTGCT AAAGGCGTCT GGTACCGGTC 1020 TGGTGCTCGC TCACTCGCTG TGACTTTAAG CAGAACCCTC CCCGAAACTT CGTTTCTTTC 1080 TTTTCTTTTC TTTTTTTTTT TTTTTTTGAA ACGGAGAGTC TCACTATGTT GCCCAGGCTG 1140 GAGTGCAGTG GCGCGAATTA GGCTCACTGC AACCTCCACC TCCTGGGTTC AAACGATTCT 1200 CCTGCCTCAG ACTCTCGAGT AGCTGAGATT AGAAACTTAG TTCCTCCATC TGTTGCATAA 1260 GGTGGTTGGC TCGGATTCTC ATCCCCAACC TCCCTTCTAC TTCGGACACA GCTACACCGG 1320 GTCGAGCAGG GAGTCGAGCT GACAACTTCG GGGCTCAGCA CCCTCTCCTA CCCCTTCGGG 1380 TCCACCTCGG CCCAGTTCGA CATGCCCGCC TCCCTCAGAT GAGTGGCCCC ACCGCACTGC 1440
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