Tag | Content |
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EnhancerAtlas ID | HS034-19809 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr22:31264220-31265700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr22:31264927-31264939 | TCTAAAAATAGT | + | 6.02 | SP8 | MA0747.1 | chr22:31265193-31265205 | AGGGGGCGTGGG | - | 6.04 |
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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 |
GH22I030868 | chr22 | 31264244 | 31265628 |
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Enhancer Sequence | GACTCAGATC CCAACCCTGC CCCTCAATAG CTGGGCACTA AGCTGGTGGC TTGGCCTCTC 60 AGAACCTGCA TTTTCTTGCC TGCAGGGAGG GAAGAATAGC CACTGTCTAC TGACCTCTAC 120 CGTGAGGCCC AGAGCAACAG CTTACGGAGC CAGTGGCCCA GACCCTGGCC CAGCCCGTGT 180 GGCCTCCAGA CGTCTGGGGG CCGCAGTTGG GCTTCTGAGT GCAGACACGC TGTGGCCTCT 240 CAATGGCCTT GCCAGGGTAG GGACTGTCCC ATCCCCAGGC AATAGATGAG GAAATTGAGG 300 CTCTGAGAGG TGAAGCCATG CTCAGGCCGC CTGGCTGGCC ACTGTCTTCC TTCTGGGCTG 360 CTGGGGCCTC CATGAGAGGG GCAGGCGGTC ATTTGAATAA CAAGTTATTG TCATTTGGGG 420 GCTGCAGTTG TGATGGGAGG CTCCCTGCCT CCTGGCTGGA TGCTGACCCA AGCCCCTGTG 480 GCCAGAGGGG GACAGGGTAT GCCGTGGGCA CCCTCCTCAG CTCCCCTTGG CTTGGGCCCC 540 ATGCAGCTGG CTGGCCTGAC CCTGCCATGG ACACCACGTG CACTCGGAAC AGTGACTCAG 600 CCATGTCCAC CCCCGTGTAC CTTGCCTGCC GTGGGAAGAA ACGTTCTCTC ACAGTATGCA 660 TTATTTTTCA AAAAAAGTCT TATATCTTGG GTTACAGATT TTCTTCATCT AAAAATAGTT 720 TTTAGCTGAT TATTTCTAAA CAAGGCATTT CAGAAACCCC TTGGCAGTTA CAGGCTCTGG 780 GACTCACTGG GTGGTGTCAG CCTCTTGGTG TCCTGTGCCA TTGTTAAACA GCAGCCTGGC 840 CCTAGGCCAG CTGCCTCCTG CCCCACCTGC TGTGGTGCGC CACCCCCCAG AGACGCCCAC 900 AGCCCCATAA CCCCAGATGC AGGCTGGGCT GGCAGGAAAG GGGCCCTGGG CAGCTGCGTG 960 AGAGAGAGGT AAGAGGGGGC GTGGGAGCTG GCAGAGGGCA CAGCCTGCCT CTCTCATGGA 1020 GGCCTCAGCA GCCCGGAAGG AAGAGGGTGG CCAGCCAGGC AGTGTGGGTA TGACTTCACC 1080 TCTCAGAGCC TCGATTTCCT CATCTGTCAC CTGGGGATGG TCCAGTCCCT ACCCTGCAAG 1140 GCCATTGAGG GGCCACAGCG TGTCTGCACA CAGAAGGCAT TCTATCAGTG AGAATGGCTG 1200 TGTTCCTGCA GGGAGATCGG TGAAGGGGAG CCTCAACTGT GACATTGGGC CTTTTGGCAG 1260 ACTTTGTTTT TGTTTGTTTG TTGTTGTGTT TTGGGTGTTT TTGTTTTGTT TTGTTTTTTG 1320 AAACAAGGTC TCATTCTGTT ACACATGCTG GAGTGCAGTG GCACGATCAT GGCTCACTAC 1380 AGCCTTCACC TCCCTGGGCT CAGGTGATCC TCCCACCTCA GCCTCCTGGG TAGCTGGGAC 1440 CATCAGCATA TGCCACTATG CCCGGCTAAT TTTTCTATTT 1480
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