Tag | Content |
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EnhancerAtlas ID | HS159-00523 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:224565410-224566770 |
Target genes | |
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 | ACCTCAAACG ATCTGCCTGC CTTGGTCTCC CAAAGTGCTG GGATTATAGG TGTGAGCCAC 60 TGCGCCTGGC CATGTAGATG ACTTTTGACC AAAATGTTTC ACCTTCTCAT TCAGATATTC 120 TTAGTAACCA AAACAGTGAC TCATGCAGTT GAGAGAGCCT TTGGGCTGTC AGTTTACAGT 180 ACATCAGGCT TGCTGAGGCT AAGCAAATCA GAAAGGTGCC ATGTTTATAA CAGAGGTCAA 240 AGCTCCTTAC TTCTGAAACA TTAGCTGTGG TTAAAAACAA AAACTCTTCC TTCTTGTATT 300 GCTTGTCTAT CAAAGCCAGG AAAGTGGGGG ATCACTGTAG TTAAATTTTT TTTTTTTTTA 360 ATTAGAGACA GAGTCTTGCC CTGTCGCCCA AGCTGGAGTG CACTGGCGCA ATCGTGGTAC 420 ACTGCAGCCT TGAACTCCTG GACTCAAGCA GTCCTCCTGC CTCAGCTTCC CAAGTAGTTG 480 GGAGTAGGTG CACACCACCA TGCCCAGCGA ATTTTTTGTA GAGACAGAGG TCTTGCTATG 540 TTGCCTAGGC TGGTATCAAA ATTACTGGCC TCAAGCGATT CTCCTGCCTC GGCCTCCCAG 600 ATGTTGGGAT TACTGGTGTG AGCCACCACG CCCAGCTCAA AAACAATTTT TTTAGGGGCA 660 CTTCTACAAA TCATGAAAGG GGGATAAAAG CACTGACTTT AAAAAGCCAT GTTTAAGATG 720 CTATAAATGT TCTCCCCTTT TCATTGATTG GAGAGTTGTA GAGGACCTTA GAGATCATTT 780 TGTCTAACTC CCTCATCCCA AAGATAAACT GAGGCCTAGA GATCGTTCAG GGTGTTGTAA 840 CTGGGAACAT CTGAATGCTG AGGCCTAGAG ATCGTTCAGG GTGTTGTAAC TGGGAACATC 900 TGAATGCTGA GGCCTAGAGA TCGTTCAGGG TGTTGTAACT GGGAACATCT GAATGCTGAG 960 GCCTAGAGAT CGTTCAGGGT GTTGTAACTG GGAACATCTG AATGCTGAGG CCTAGAGATC 1020 GTTCAGGGTG TTGTAACTGG GAACATCTGA ATGCTGAGGC CTAGAGATCG TTCAGGGTGT 1080 TGTAACTGGG AACATCTGAA TGCTGAGGCC TAGAGATCGT TCAGGGTGTT GTAACTGGGA 1140 ACATCTGAAT GCTGAGGCCT AGAGATCGTT CAGGGTGTTG TAACTGGGAA CATCTGAATG 1200 CTGAGGCTTA GTCCAGTGTT CTCTCTCCCT TACCACTCCT CTTCCCCTTC CCTCTATAAT 1260 GGCAGTACCC AGGGCCCGGT CCATAGACTA CTATCGAGTG CTCCTATGTG CATCTTAGTA 1320 CGTATCATTT TCCCTTGCCT TTTTCCTTCT ATCCTTTCAG 1360
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