Tag | Content |
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EnhancerAtlas ID | HS050-10799 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:889850-891770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr11:891308-891319 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr11:891308-891318 | GCCCCGCCCC | + | 6.02 | SP3 | MA0746.2 | chr11:890456-890469 | GGCCCCGCCCACC | + | 6.14 | Zfx | MA0146.2 | chr11:890015-890029 | CAGGCCTAGCCCGC | - | 6.38 | Zfx | MA0146.2 | chr11:890118-890132 | CAGGCCTAGCCCGC | - | 6.38 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr11 | 890776 | 891180 | chr11 | 890116 | 890247 | chr11 | 890149 | 890200 | chr11 | 891232 | 891564 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I000890 | chr11 | 890261 | 890410 |
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Enhancer Sequence | AGCCAGCGGC CACAGCTGTT CCTCCACCCA CAGCTCCCCT CCCCCTCTGC CCACCTGTCA 60 GAGATTTCTG AACCCGCTCC CCATGGCCTT GGGTCGCCTG GCCCCTGTCT GCTGCTGCTG 120 GCATCCTCGC CCCCTCACGA TGGCTGCTCT ACTGTTCTCA GCCTGCAGGC CTAGCCCGCT 180 CCCCATGGCC TTGGGTCCCC TGGCCCCTGT CTGCTGCTGC TGGCGTCCTC GCCCCCTCAC 240 GATGGCTGCT CTACTGTTCC TCAGCCTGCA GGCCTAGCCC GCTCCCTGAC TGGCCGGTTA 300 GCACCCTTTG GCCCTTTGGG GCCTGACCTC AGCCTGGACC TCGGCCCGTC CACACCGCAC 360 GGGGTGCCTA CGGTCCCCCA CAGAGGCCTC AACACACACT GCCAGCACGC GGCCTGCCCC 420 ATCCCCTGAG GCTGCGGGCA AGAGGCAGGT GGGCGACGGG AGCAGGGGCC TCTGTGCAAA 480 CGTGCTTGCT GGGGATACGG TGACGGCGCC CCCATGCGTC ACCTTTCTCT GACTGCTGAG 540 TTGGGCTCCA CATATAGCGA TGGCCGGCCC TGAACCACGG GGCTTGCAGG AGCTGGCCAG 600 GGTCGCGGCC CCGCCCACCT CAGAGTGGAC CACTGACAAC AAGGCCGGCA ACGGCGCCAG 660 CAGGGCCCAG GAAGGAAACC AGCCCTTCCT GGGTTCCTGA GGTCAGCTCC CTGGACCCAA 720 GGGGGTCCCA GTAGCTAACA ATGCCCAGAA AACACAAGGG GCCAACTAGA GAGTGACCCA 780 AGGGTTCTGC TCCCATGTTA AGGATGGCAC CACCACATGG GCACCTGGGG ACAGCCTGTT 840 GGTCCCACTG GCCTGTGGGG TTTACGCTGT GGCTTTGCCC CTGGGTCTCC TCCATTGCTG 900 AGACTGACTG TGGGAGCAGG GCTGGAGGTC CGCAGAGTGC TCAGTTCCAG GACCAGACAC 960 CCTGGGGTCT GTGGCAGCTG AGTTAGGGCT GCCTCTGTCT GCTGACGAAG GACACGATAA 1020 AATTGGCATT TGGCGACTGG GGTGCCCCTC CCCGCAGCAC GCAGACCTCT CTCCAGGGGC 1080 CATTGTTCCA CAGACAGTGC CCCTGGAGAG AGCGAGCCTG TGTGCTGGCA GCGCTGCTCT 1140 TGGGAGGTGA GTGACAAGCA CAATTACGCG CTGCTGCAAA AGCACCAGGG ACAGGGATTT 1200 ACGAGGCTCC TCTGCAGTGG CTGCTCTTCC CTCAGAGTGG GATGGGGGAA GGATAAACAG 1260 ATGACAAAAC AGCCCTCCTC ACCTCTGGGG CTGTAGCCAG AGTCTCGGGA GAACCCACGG 1320 GAGCCTCAGC ACCTTCACCG GCCCCGCCGA CTGGGAGGGC ACAGCCCTGT GCTCCAGTGG 1380 AGCGGGCGCA CAACAGCAGT GCCCAGCCCT CCCCCGAGCT GGGTCCCACT TCCCCGGGGA 1440 CCCCCACCGT GGGCCTCGGC CCCGCCCCCA GCCTCGTCAC CGTGCCCGTA GCCCTGGCGT 1500 GCATCCCACC CTACAGCTGC AACCCCCACC AGCGCCATGC AAATGGAGTT GTGAGCTTTG 1560 GTTGCTGTGG GGTGAGGGGC AGGGACCTGG CCCAGCTCCA ACTGCCCACT TCCTGCCTAG 1620 GGCCAGAAGC TCAGGCAGAG GCTGCCACCA GCAGAAGACA GGCACCTGGT CCTCTGCCCC 1680 AGCCTCAAGA ACTGCCCTGG GCTCCTGAGC TGGTCCCCAC CGATGGCTGC TTCTGCAGCT 1740 CCCCTAAGCA CAAAGGGCAA CCTGGGAGCC CCATGAAATC AGTGCCTCAC AGAGGTGGCC 1800 ATGCCCATGG CCTCTGGACA AGGAGTGTCT GCTGCCCCGA GGAATCTTCA CCCAGCCCCA 1860 GGCCTGTAGT CCTCCCAACC ACCTGAGACA GGTGCTGTCA GCTCTGGAAG GACGTGTCCT 1920
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