Tag | Content |
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EnhancerAtlas ID | HS082-01442 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:92389180-92390620 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:92389724-92389745 | ACCATCTTTTACTTTCATTTT | + | 6.1 | MYCN | MA0104.4 | chr1:92389851-92389863 | GACCACGTGGCC | + | 6.52 | MYCN | MA0104.4 | chr1:92389851-92389863 | GACCACGTGGCC | - | 6.52 | RREB1 | MA0073.1 | chr1:92390180-92390200 | CCCCCACCCACCCACACACA | + | 8.61 |
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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 |
GH01I091923 | chr1 | 92389391 | 92390469 |
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Enhancer Sequence | CCTGCCTCAG CCTCCCGTGT AGCTGGGACT ACAGGCGCGC GCCACCATGC CCGGCTAATT 60 TTTGTATTTT TAGTAGAGAC GGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG 120 ACCTCGTGAT CCGCCCGTCT CGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCG 180 CGCCCGGCCA GGAATAACTT CCTATGTGTC TGTGGGTCCT GCATCACCCC AAACATGTCC 240 TTCCACTCTG CATTCTTCCC CTGAATTAGT CACTCTCATA ATCCATTTTA GTAAAGCATC 300 CTCAGGAAGC CAATGACACC AGTCTACAAA ATGGAACGAT TCCTTCACAC TCTCCTTCTG 360 GTTTCAATAG TTACTTGGTT TTGCCCTTCC TTCACATTGA CTACCTTCTT GGTAACCACA 420 GATCTCAGAG GCACATTCTG TTGTCCCTGT ATAATTTTCT CCTTTGTGGG TGACTTTGAG 480 GCTAGTGGCC TGAGCTCAGA CAGACCCACA TCTGAGGTTG GTCAGCCTCA AGTCCTGACC 540 CAGCACCATC TTTTACTTTC ATTTTAGCCA TTGCAGATAA CAATAACCAA TGAATTAAAT 600 ATCTTAACTC CACTTGTAAC TTTTACCTTT AGTAACTGAT CTCAACACAG CTGTGGCTTC 660 ATACCGTGGG TGACCACGTG GCCACCCAGA AATCAAAGAT TTCTCATCCC CACCCTTTTA 720 TTGTTTCTCT TCCCAAACCA CATGTTTCCA TGAGTCAGAG CCATTCCAGC AAATCCTGCT 780 TCACTGACAT CAGTTGTGTA GGGAAAACTC TAACTGTGTT TTTCCTCTAC TCTCACACCA 840 CAACAATCAT CAACACAAAA GGAGACTTCT GTGACCATAT GTATGGGTTT ATTTTCCCCT 900 GGACACCAAG CAGTGGACAC CATCTGGGTG TCTTCTAATT CAGTTCCAAC ACTGTCTACC 960 GGAATAGTGT CAGATCCCAC AGGTTGAGAC CAAGACTGGC CCCCCACCCA CCCACACACA 1020 CCAGTCTCAC GTCCAGGCCT CCAGAACTTC TAACCAACTG GCTTCAAGTT GGGGTTCCTA 1080 TGTCCCCCTC TTTGAGTTTG ATTAATTCGC TGGAGTGGCT CACAGAACTC AGGGAAACAC 1140 TTACTTGTGT TTACCGGTTT ATTATAAAGC ATATTGCAAA GGATACAGAT GAAGAAACAC 1200 GTAGGGCAAA GTATGGGTGA AGGGTGTGGA GTTTCCATGC CCTCCCTGGG TGCGCCACCC 1260 TCCAGGAACC TCTGTGTGTT CAGCTGTCTG GAATCTCTGT ATCATCAATT TCTGCCTCCA 1320 TTTTCACATG GTCTTCTCCA CTTTTGTCTG TGTTTGTCCT CTGAGTGTCT CTTATAAGGA 1380 CACTTGTCAT TGGATTTAGG ACCCACTTGG ATAACCCAGA ATGAGCTAAT TTGAAGATTT 1440
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