Tag | Content |
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EnhancerAtlas ID | HS196-04571 |
Organism | Homo sapiens |
Tissue/cell | ZR75-1 |
Coordinate | chr1:224565320-224566770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:224565766-224565776 | TTTAATTAGA | - | 6.02 | FOSL1 | MA0477.1 | chr1:224565544-224565555 | AGTGACTCATG | + | 6.14 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I224376 | chr1 | 224564092 | 224568999 |
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Enhancer Sequence | GGGATTACGG CTAGCTACTC CTGGCTAATT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC 60 CATGTTGGCC AGGCTGGTCT CAAACTCCTG ACCTCAAACG ATCTGCCTGC CTTGGTCTCC 120 CAAAGTGCTG GGATTATAGG TGTGAGCCAC TGCGCCTGGC CATGTAGATG ACTTTTGACC 180 AAAATGTTTC ACCTTCTCAT TCAGATATTC TTAGTAACCA AAACAGTGAC TCATGCAGTT 240 GAGAGAGCCT TTGGGCTGTC AGTTTACAGT ACATCAGGCT TGCTGAGGCT AAGCAAATCA 300 GAAAGGTGCC ATGTTTATAA CAGAGGTCAA AGCTCCTTAC TTCTGAAACA TTAGCTGTGG 360 TTAAAAACAA AAACTCTTCC TTCTTGTATT GCTTGTCTAT CAAAGCCAGG AAAGTGGGGG 420 ATCACTGTAG TTAAATTTTT TTTTTTTTTA ATTAGAGACA GAGTCTTGCC CTGTCGCCCA 480 AGCTGGAGTG CACTGGCGCA ATCGTGGTAC ACTGCAGCCT TGAACTCCTG GACTCAAGCA 540 GTCCTCCTGC CTCAGCTTCC CAAGTAGTTG GGAGTAGGTG CACACCACCA TGCCCAGCGA 600 ATTTTTTGTA GAGACAGAGG TCTTGCTATG TTGCCTAGGC TGGTATCAAA ATTACTGGCC 660 TCAAGCGATT CTCCTGCCTC GGCCTCCCAG ATGTTGGGAT TACTGGTGTG AGCCACCACG 720 CCCAGCTCAA AAACAATTTT TTTAGGGGCA CTTCTACAAA TCATGAAAGG GGGATAAAAG 780 CACTGACTTT AAAAAGCCAT GTTTAAGATG CTATAAATGT TCTCCCCTTT TCATTGATTG 840 GAGAGTTGTA GAGGACCTTA GAGATCATTT TGTCTAACTC CCTCATCCCA AAGATAAACT 900 GAGGCCTAGA GATCGTTCAG GGTGTTGTAA CTGGGAACAT CTGAATGCTG AGGCCTAGAG 960 ATCGTTCAGG GTGTTGTAAC TGGGAACATC TGAATGCTGA GGCCTAGAGA TCGTTCAGGG 1020 TGTTGTAACT GGGAACATCT GAATGCTGAG GCCTAGAGAT CGTTCAGGGT GTTGTAACTG 1080 GGAACATCTG AATGCTGAGG CCTAGAGATC GTTCAGGGTG TTGTAACTGG GAACATCTGA 1140 ATGCTGAGGC CTAGAGATCG TTCAGGGTGT TGTAACTGGG AACATCTGAA TGCTGAGGCC 1200 TAGAGATCGT TCAGGGTGTT GTAACTGGGA ACATCTGAAT GCTGAGGCCT AGAGATCGTT 1260 CAGGGTGTTG TAACTGGGAA CATCTGAATG CTGAGGCTTA GTCCAGTGTT CTCTCTCCCT 1320 TACCACTCCT CTTCCCCTTC CCTCTATAAT GGCAGTACCC AGGGCCCGGT CCATAGACTA 1380 CTATCGAGTG CTCCTATGTG CATCTTAGTA CGTATCATTT TCCCTTGCCT TTTTCCTTCT 1440 ATCCTTTCAG 1450
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