Tag | Content |
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EnhancerAtlas ID | HS094-17805 |
Organism | Homo sapiens |
Tissue/cell | hMADS-3 |
Coordinate | chr18:12414950-12416560 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr18:12415104-12415120 | TTTTGTTGACATAGGG | - | 6.19 | Zfx | MA0146.2 | chr18:12415499-12415513 | CCCGCCTCGGCCTC | + | 6.01 |
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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 |
GH18I012415 | chr18 | 12415321 | 12416199 |
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Enhancer Sequence | ACGGTCTTGC TCTGTTGCCC AGGCTGGAGT GCAGTAGTGC AATCACGACT TACTGCAGCC 60 TCAAACTGTT TGGCTTAAGT GATCCTCCCA TCTCAGGCTC TGCAGTAGCT GGGACTATGG 120 TTGCGAGCTA CCACACCTGG CTAATTTTCG TATTTTTTGT TGACATAGGG ATCTTGCTCT 180 ATTGCGCAGG CTGGTCTTGA ACTCCTGGTC TCAAGTGAAC TTCCTGCCTT GGCCTCCCAA 240 AATGCTGGGG TTACAAGCAT AAGCCAACAC ACCTGGTCTG CCTACATCTT TTTTTTTTTT 300 TAATTTTTAT TTTTTTGTTT TGTTTTGAGA CAGGGTCTCA CTCTGTCACC CAGGCAGAAG 360 TGCAGTGGTG CGTTCTTGGC TCACAGCAAC CTCTGCCTCC CAGGTTCAAG CAATTCTCCT 420 GCCTCAGGCT CCTAAGTAGC TGGGACTACA GGTGTGCGCC ACCATGCCCA GCTAATTTTT 480 GTATTTTTAG TAGAGACTGG GTTTCACCAT GTTGGGCAGG CTGTTCTAGA ACTCCTGTCA 540 AGTGATCCGC CCGCCTCGGC CTCCCAAAGT GCTGGGATTA CAGGCATGAG CCACTGTGCC 600 TGGCCTTAAA TCTTTTTAAG ACAGATTTTT GCTATGGAAA TTTCACAACT ATGCAAACAT 660 GGAGAGACTA GAATACTGAG AGCCGGTGCC ACCCCCAGCT TAACAGTTAC CCTCTGGCAG 720 CCAGTCCAGG GTCCTCTGTG TCCCCACCCA CTGCTCCTTC CCCTGGGTTA TTTTAGGCAA 780 ATCCCAGACA TCATGTAATT TCCTCCTTCT TCATCTTCCC GACACTGTTG GTGCTTAGAG 840 AGTCCTTTGT TATTCCTTTT CATTCCCCAG CTCAGAAACC AGCTTCCCTT AGCCCGCCAG 900 GCAGACCCAC CACACACATG GTGTCAGAGC ACTTGGGACA CGTGTATGTG GGGAGCCATC 960 CATGCTGGGT GGCAGCGGAG GCCTCTTGCC CTTGGGGGAT AGGATTCCCC AGAGGTCTCC 1020 ACGAACAGCA GCAGAGGAGG CTCCTGCCGC CTGGTTGGGG ATCTCTGAGT AGGCAGTTCT 1080 CTGCTCCTCT TGAAAATAAA CTTCAGCACA TTCCTCTTCT GCCTCAACCA GGCAGCTGAG 1140 AACCCTGACT GATTTCGGCA GGGGCGGGGT GTCCATTTTC AGCTTCTCTG GGTAAACTGC 1200 TGCCATTAGT GCCTGTGCCA GTTTGTGTCC ACCAGCAGCA CTTCCTGTTG TCCTATTTCC 1260 TATACCCTTT CCAGTACTCA ATATTGCCAG ACTTGTCTAT TTTTGCCCAT TGAAAGCGTG 1320 TCAGGCTATT TTTGTTCTTT CTGGGTTTTT GTTGTTGTTG TTGTTGTTTG TTTTTTTAGA 1380 CAGGCATTTG CTCTGTCACC CAGGCTGGAG TGCAGTGGTA CAATCATGGC TTGCTGCAGC 1440 CTCGACCTCC GGTCTTAGGT GATCCTCCTG CCTCAACCTC AGCCTCCCAA ATAGCTAGTA 1500 CCACAGGGGT GTGCCACCAT GCCTGGTTAA TGTTTTCTGT TTTTGTAGAG ATGAGGGGTC 1560 TTGCTATATT GCCCAGGCTG GGCTTGAGCT CCTAGCATCA AGCAGTCTTC 1610
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