Tag | Content |
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EnhancerAtlas ID | HS105-01265 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:23176870-23178310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr1:23178211-23178226 | CCTGGCCTTGAACCT | - | 6.86 | ZBTB18 | MA0698.1 | chr1:23176978-23176991 | CAGCCAGATGTGC | + | 6 | Zfx | MA0146.2 | chr1:23176995-23177009 | GGGGCCTGGGCCTG | + | 6.73 |
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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 |
GH01I022851 | chr1 | 23178080 | 23178304 |
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Enhancer Sequence | TTTGGGAGAT GCTCCCCAGC TCCGCCAGGT CCATCTCACC CTCACGGTAC CAGGACTGGG 60 CCTGCCAGGC CTTACCTCGG TGGCCCACTA CACCACCTGT CAATACAGCA GCCAGATGTG 120 CGGGAGGGGC CTGGGCCTGG CCCTGCCAGA TGTGTCAAGC TTTGCAAACA CATCCGACTT 180 CCCCTCGGGC ACATCGTGAT TATTGTTTAA CACTCGCTAT TCCTGCATCT GTGAGTCCCA 240 GGGATTACAG GCTGGGAGGC TGCAGCCTGA TGAGCCCACT GGCAGTGATA GTCTCCAGCT 300 GGGGAGAAGG GGATACTCGA TCGGTCCCCA TTTTCTCAGG AGGGTGAGGG ATGTGGCATG 360 AACCCCAAAT ATAGATGAGG AGATGAGGCC CGGAGAGAGG CTCAGGGAAG AACTGATGGA 420 ACCAGGACTT GAACCAGGCA GGAGAAACGG CGCATGCACA GGCCCTGAGG CTAGCAGAAG 480 GCTGGTGTTC TCAGGGCAGC CAAGAGGTCA GTGTGGCTCA GCTGGAGTGG GCAAGAGGCC 540 AGGCGGGTGG AGGGGAGTTC AGAGAGGAAA AAGGAAGCTT TGTAGGCTAT TGTTTTGTGG 600 GTTTTTGTTT CTTTTTGGAA ATTCATCTTT GTTTAGATAC AGGGTCTTGC TCTGTTGCCC 660 AGATTGGAGT GCAGTGGTGG GCTCTCAGCT CACTGCAACC TGAACCTCCC AGGCTCAAGA 720 GATCCTCCCA CCTCAGCCTC CCAAGTAACT GGGACCACAG GCTTGTGCCA CCACGCCCAG 780 CTCATTTTTT AAAATTTTTT TGTAGAGTCA AGGTCTCACT ATGTTGCTCA GACTGGTCTC 840 AAACTCCTCA GCTCAAGCGA TCCTCCCGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGT 900 GTGAGCCACC GTGCCCAGGC TATTGGTTTT TACTCCAAGT GAGATGGAAA CTGTTGGAGG 960 CCTTTGGGCG ACATGAGCTG ATGGCTGTTC TGCAGGATCC TGGCTGCTGT GGAAGGCTGA 1020 ATGCAGCTGG AGGAGGGCAA GGACATGGGA GAGCAAGGGA GAAAGCCAGG AAGCCAGTTA 1080 GGCTTTTGCC GTGATGTGAG GATGCTCCCA CTCCTCTGCC CCTTCTCTTC CCTCCAATGT 1140 GGGCATCAGC ATAGCTGGGC TGCAACCCCA GCTCTGCTGG CCACTCATTT ATTGTGTGAC 1200 CTTAGGCAAG TCCCTGTCCC TGTCTGGGTC TTGTATTTTG TAGTCATAAA ATAAGGAACT 1260 TAGCCCAGAA GATCGTGAAG ATTCTGCTGA CTTCCAATGT CTGAGACCCT GCCTTACTCT 1320 CCAGCCTCAT CTCCTTCCTC TCCTGGCCTT GAACCTCACG TGCTAGCAAC CCTGAACTAT 1380 TTGTAGCTCT CTGCACGCAC ACCATGCTGT TTCACGCCTC TGTGCCTTTG CACACTCCCT 1440
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