Tag | Content |
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EnhancerAtlas ID | HS050-69472 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr9:97737410-97739110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr9:97737681-97737702 | TATTTGTTTCACTTTTAGTGC | + | 6.08 | MSC | MA0665.1 | chr9:97738706-97738716 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr9:97738706-97738716 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr9:97738706-97738716 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr9:97738706-97738716 | AACAGCTGTT | - | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 97738128 | 97738262 | chr9 | 97738417 | 97738842 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I094976 | chr9 | 97738481 | 97738630 |
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Enhancer Sequence | GCTGAGATGG GAGGATCGTT TCATCCCTGG AGGAGGAGGA GGTTGTTGCA GTGAGCTGAG 60 ATTGAACCAC TGCACTCCAG GCTGAGTGAC AAAGTGGGAC TCTGTCTCTA ATAATAATAA 120 TAATAATAAG TAATAATAAT AATATTGGTC TTGCACAGTT ATTGTCAAGT ATAGATGATA 180 CTCTGTCTAT TGTGTCTGGC ACACAGTAGG TGTTCAATAA GCAGTAGCTT CTAGTTTTAT 240 GCCTTTTCTT GGCAGTGGAT AGAGGACTTT TTATTTGTTT CACTTTTAGT GCCACGGTAG 300 AATAGTGTCT GTGTGTGCAA GTACTAACTA TGTTAAAGCA GAATTTGCCA ATGAACTAAC 360 CCTCTGAGTT GGCCGAAGAC TGTGGCACAG GCAAATTGTA TGCAGCCACA TGCTTCCTAC 420 GGAAAGTCAT CCTGCAGAGA TTCCTGGGGC CCACTATCTG CACAGTGTCT CCCAACCCTG 480 CAGCTGGACT GCTTCAGTGC TGCCCTGCAG ATCCGTCCCC TGCACGCCAC ATCCATGTGG 540 GCCGCTCTCG TTGCCTCCTG CAGAAACATT CTGCAAGTTC TGGTGTGGTC TCCCTGCCTC 600 CAGCCTCTTC TCCGCTTTTT CTTCCTTGAC TCAGTTCTCT GCCGTGTCCC TCTGCAATTT 660 TGCTCCAGAG CCTCCTTGAC AAAGGCAGGG CCCGGTAGCA GGGACTGCAG AGTCCCCGCA 720 GGACCCGCTG TTTTCTTTCT CAGCTCATTC TGGAGGCCAG CCCCACTGAG CTGAACGGAG 780 TCTGCACACT ACTGCACTGG CATTCCTGCT CCTGCTATCT TTGCCCCGAT GTGCTTTTCT 840 TCCATTTCTA TTGGCTTTGC CCCACCAGGA CCCAGTCATG CATGGCCTTC TTAGGAAGCC 900 TCTCCTGATG CACCTCCTCT TGTCCTGTTT TACCTATCCC ACCTGCAGCA GTGGTTCTTC 960 AACACCTAGA GGACCATCAT CTCTACAGGC GCTGGTAGCA TTCTGCCTGG TGTCTATTAC 1020 ACATCCCTAA TCCACAGTCA CTCCCTGGGT TTTCCCATCC CAGCCTTCCA CAGAACCTTT 1080 GCCCAGCAGC CATCCAGCGA ATGTTTGCCA CATAGAGAAT GTTGCCTGTT TTTCAGTCTT 1140 CTCTGGTGAA GACTTTGGAC CTCACTTAAT AACATTCCAG GGCTCAACTC CCCAGCCCCC 1200 ACTCCATGCC ACCCCTAGAG AAGCATCTGT AAGTGAAAAT TCCCCAAAGG AAATTTATGT 1260 CCGTGTCTTC ATATTCACTC CCCCATGCTG ATACACAACA GCTGTTCACT GTCTTTTGTA 1320 AAATCACTCA AAAATAGCAA TTAAGTCGCT CCTCGGACTT CTCTTCTCTG GGATATTTAA 1380 CCTCAGTTCC CTTTACCTCC CTTGTGGGCT CTTCCCCTTT TGATCGTCAC TATTGCTCTC 1440 TCTAAGTCCT TTCCAAATTC TGCATCTTCC TCTTAAATAT CTTATGGGAA AGGTGGAGAC 1500 TTGTTTTCAG TTCAGAAGAC AGCCTCTTTT TTTTTTTTTT TTTCTTTTTG GGGGTTTGAG 1560 ACAGGGTCTC ACTTTGTCCC CAGGCTGGAG TGTAGTGGTG TGATCCAGGC TCACTGCAAC 1620 CTCTGCCTCC CAGGCTCAAG CCATTCTCCC ACCTCAGCCT CCCAAATAGC TGGGACTATA 1680 TGCACATGCC ACCATGCCCA 1700
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